Canonical Allele Identifier: CA343772053
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873043T>A (hg19) chr1:g.173903905T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903905T>A , CM000663.2:g.173903905T>A GRCh38
NC_000001.10:g.173873043T>A , CM000663.1:g.173873043T>A GRCh37
NC_000001.9:g.172139666T>A NCBI36
NG_012462.1:g.18474A>T , LRG_577:g.18474A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1379A>T MANE Select ENSP00000356671.3:p.Asn460Ile
ENST00000367698.3:c.1379A>T ENSP00000356671.3:p.Asn460Ile
ENST00000617423.4:c.764A>T ENSP00000478688.1:p.Asn255Ile
NM_000488.3:c.1379A>T , LRG_577t1:c.1379A>T NP_000479.1:p.Asn460Ile
XM_005245198.2:c.1235A>T XP_005245255.1:p.Asn412Ile
NM_001365052.1:c.1235A>T NP_001351981.1:p.Asn412Ile
NM_000488.4:c.1379A>T MANE Select NP_000479.1:p.Asn460Ile
NM_001365052.2:c.1235A>T NP_001351981.1:p.Asn412Ile
NM_001386302.1:c.1502A>T NP_001373231.1:p.Asn501Ile
NM_001386303.1:c.1460A>T NP_001373232.1:p.Asn487Ile
NM_001386304.1:c.1358A>T NP_001373233.1:p.Asn453Ile
NM_001386305.1:c.1322A>T NP_001373234.1:p.Asn441Ile
NM_001386306.1:c.1163A>T NP_001373235.1:p.Asn388Ile
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