Canonical Allele Identifier: CA343774576
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879001G>C (hg19) chr1:g.173909863G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909863G>C , CM000663.2:g.173909863G>C GRCh38
NC_000001.10:g.173879001G>C , CM000663.1:g.173879001G>C GRCh37
NC_000001.9:g.172145624G>C NCBI36
NG_012462.1:g.12516C>G , LRG_577:g.12516C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.842C>G MANE Select ENSP00000356671.3:p.Ala281Gly
ENST00000367698.3:c.842C>G ENSP00000356671.3:p.Ala281Gly
ENST00000487183.1:n.493C>G
ENST00000617423.4:c.559+2001C>G ENSP00000478688.1:n.559+2001C>G
NM_000488.3:c.842C>G , LRG_577t1:c.842C>G NP_000479.1:p.Ala281Gly
XM_005245198.2:c.698C>G XP_005245255.1:p.Ala233Gly
NM_001365052.1:c.698C>G NP_001351981.1:p.Ala233Gly
NM_000488.4:c.842C>G MANE Select NP_000479.1:p.Ala281Gly
NM_001365052.2:c.698C>G NP_001351981.1:p.Ala233Gly
NM_001386302.1:c.965C>G NP_001373231.1:p.Ala322Gly
NM_001386303.1:c.923C>G NP_001373232.1:p.Ala308Gly
NM_001386304.1:c.821C>G NP_001373233.1:p.Ala274Gly
NM_001386305.1:c.785C>G NP_001373234.1:p.Ala262Gly
NM_001386306.1:c.626C>G NP_001373235.1:p.Ala209Gly
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