Canonical Allele Identifier: CA343774216
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878914T>G (hg19) chr1:g.173909776T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909776T>G , CM000663.2:g.173909776T>G GRCh38
NC_000001.10:g.173878914T>G , CM000663.1:g.173878914T>G GRCh37
NC_000001.9:g.172145537T>G NCBI36
NG_012462.1:g.12603A>C , LRG_577:g.12603A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.929A>C MANE Select ENSP00000356671.3:p.Asp310Ala
ENST00000367698.3:c.929A>C ENSP00000356671.3:p.Asp310Ala
ENST00000487183.1:n.580A>C
ENST00000617423.4:c.559+2088A>C ENSP00000478688.1:n.559+2088A>C
NM_000488.3:c.929A>C , LRG_577t1:c.929A>C NP_000479.1:p.Asp310Ala
XM_005245198.2:c.785A>C XP_005245255.1:p.Asp262Ala
NM_001365052.1:c.785A>C NP_001351981.1:p.Asp262Ala
NM_000488.4:c.929A>C MANE Select NP_000479.1:p.Asp310Ala
NM_001365052.2:c.785A>C NP_001351981.1:p.Asp262Ala
NM_001386302.1:c.1052A>C NP_001373231.1:p.Asp351Ala
NM_001386303.1:c.1010A>C NP_001373232.1:p.Asp337Ala
NM_001386304.1:c.908A>C NP_001373233.1:p.Asp303Ala
NM_001386305.1:c.872A>C NP_001373234.1:p.Asp291Ala
NM_001386306.1:c.713A>C NP_001373235.1:p.Asp238Ala
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