Canonical Allele Identifier: CA343773943
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878848G>T (hg19) chr1:g.173909710G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909710G>T , CM000663.2:g.173909710G>T GRCh38
NC_000001.10:g.173878848G>T , CM000663.1:g.173878848G>T GRCh37
NC_000001.9:g.172145471G>T NCBI36
NG_012462.1:g.12669C>A , LRG_577:g.12669C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.995C>A MANE Select ENSP00000356671.3:p.Thr332Asn
ENST00000367698.3:c.995C>A ENSP00000356671.3:p.Thr332Asn
ENST00000617423.4:c.559+2154C>A ENSP00000478688.1:n.559+2154C>A
NM_000488.3:c.995C>A , LRG_577t1:c.995C>A NP_000479.1:p.Thr332Asn
XM_005245198.2:c.851C>A XP_005245255.1:p.Thr284Asn
NM_001365052.1:c.851C>A NP_001351981.1:p.Thr284Asn
NM_000488.4:c.995C>A MANE Select NP_000479.1:p.Thr332Asn
NM_001365052.2:c.851C>A NP_001351981.1:p.Thr284Asn
NM_001386302.1:c.1118C>A NP_001373231.1:p.Thr373Asn
NM_001386303.1:c.1076C>A NP_001373232.1:p.Thr359Asn
NM_001386304.1:c.974C>A NP_001373233.1:p.Thr325Asn
NM_001386305.1:c.938C>A NP_001373234.1:p.Thr313Asn
NM_001386306.1:c.779C>A NP_001373235.1:p.Thr260Asn
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