Canonical Allele Identifier: CA343772551
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873139T>C (hg19) chr1:g.173904001T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904001T>C , CM000663.2:g.173904001T>C GRCh38
NC_000001.10:g.173873139T>C , CM000663.1:g.173873139T>C GRCh37
NC_000001.9:g.172139762T>C NCBI36
NG_012462.1:g.18378A>G , LRG_577:g.18378A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1283A>G MANE Select ENSP00000356671.3:p.Asn428Ser
ENST00000367698.3:c.1283A>G ENSP00000356671.3:p.Asn428Ser
ENST00000617423.4:c.668A>G ENSP00000478688.1:p.Asn223Ser
NM_000488.3:c.1283A>G , LRG_577t1:c.1283A>G NP_000479.1:p.Asn428Ser
XM_005245198.2:c.1139A>G XP_005245255.1:p.Asn380Ser
NM_001365052.1:c.1139A>G NP_001351981.1:p.Asn380Ser
NM_000488.4:c.1283A>G MANE Select NP_000479.1:p.Asn428Ser
NM_001365052.2:c.1139A>G NP_001351981.1:p.Asn380Ser
NM_001386302.1:c.1406A>G NP_001373231.1:p.Asn469Ser
NM_001386303.1:c.1364A>G NP_001373232.1:p.Asn455Ser
NM_001386304.1:c.1262A>G NP_001373233.1:p.Asn421Ser
NM_001386305.1:c.1226A>G NP_001373234.1:p.Asn409Ser
NM_001386306.1:c.1067A>G NP_001373235.1:p.Asn356Ser
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