Canonical Allele Identifier: CA343772056
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873044T>A (hg19) chr1:g.173903906T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903906T>A , CM000663.2:g.173903906T>A GRCh38
NC_000001.10:g.173873044T>A , CM000663.1:g.173873044T>A GRCh37
NC_000001.9:g.172139667T>A NCBI36
NG_012462.1:g.18473A>T , LRG_577:g.18473A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1378A>T MANE Select ENSP00000356671.3:p.Asn460Tyr
ENST00000367698.3:c.1378A>T ENSP00000356671.3:p.Asn460Tyr
ENST00000617423.4:c.763A>T ENSP00000478688.1:p.Asn255Tyr
NM_000488.3:c.1378A>T , LRG_577t1:c.1378A>T NP_000479.1:p.Asn460Tyr
XM_005245198.2:c.1234A>T XP_005245255.1:p.Asn412Tyr
NM_001365052.1:c.1234A>T NP_001351981.1:p.Asn412Tyr
NM_000488.4:c.1378A>T MANE Select NP_000479.1:p.Asn460Tyr
NM_001365052.2:c.1234A>T NP_001351981.1:p.Asn412Tyr
NM_001386302.1:c.1501A>T NP_001373231.1:p.Asn501Tyr
NM_001386303.1:c.1459A>T NP_001373232.1:p.Asn487Tyr
NM_001386304.1:c.1357A>T NP_001373233.1:p.Asn453Tyr
NM_001386305.1:c.1321A>T NP_001373234.1:p.Asn441Tyr
NM_001386306.1:c.1162A>T NP_001373235.1:p.Asn388Tyr
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