Canonical Allele Identifier: CA10728634
Community Standard Title: NM_001924.4(GADD45A):c.384+118T>C
Gene: GADD45A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67686705T>C , CM000663.2:g.67686705T>C GRCh38
NC_000001.10:g.68152388T>C , CM000663.1:g.68152388T>C GRCh37
NC_000001.9:g.67924976T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001924.4:c.384+118T>C MANE Select NP_001915.1:n.384+118T>C
ENST00000370986.9:c.384+118T>C MANE Select ENSP00000360025.4:n.384+118T>C
NM_001199741.1:c.282+118T>C NP_001186670.1:n.282+118T>C
NM_001199741.2:c.282+118T>C NP_001186670.1:n.282+118T>C
NM_001199742.1:c.146+579T>C NP_001186671.1:n.146+579T>C
NM_001199742.2:c.146+579T>C NP_001186671.1:n.146+579T>C
NM_001924.3:c.384+118T>C NP_001915.1:n.384+118T>C
ENST00000370985.3:c.282+118T>C ENSP00000360024.3:n.282+118T>C
ENST00000370985.4:c.282+118T>C ENSP00000360024.3:n.282+118T>C
ENST00000370986.8:c.384+118T>C ENSP00000360025.4:n.384+118T>C
ENST00000617962.1:c.146+579T>C ENSP00000482814.1:n.146+579T>C
ENST00000617962.2:c.330+118T>C ENSP00000482814.2:n.330+118T>C
ENST00000648742.1:c.45-956T>C ENSP00000497697.1:n.45-956T>C
ENST00000650283.1:c.146+579T>C ENSP00000496875.1:n.146+579T>C
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