Canonical Allele Identifier: CA343772010

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873035C>A (hg19) ; chr1:g.173903897C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903897C>A , CM000663.2:g.173903897C>A	GRCh38
NC_000001.10:g.173873035C>A , CM000663.1:g.173873035C>A	GRCh37
NC_000001.9:g.172139658C>A	NCBI36
NG_012462.1:g.18482G>T , LRG_577:g.18482G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1387G>T MANE Select	ENSP00000356671.3:p.Val463Phe
ENST00000367698.3:c.1387G>T	ENSP00000356671.3:p.Val463Phe
ENST00000617423.4:c.772G>T	ENSP00000478688.1:p.Val258Phe
NM_000488.3:c.1387G>T , LRG_577t1:c.1387G>T	NP_000479.1:p.Val463Phe
XM_005245198.2:c.1243G>T	XP_005245255.1:p.Val415Phe
NM_001365052.1:c.1243G>T	NP_001351981.1:p.Val415Phe
NM_000488.4:c.1387G>T MANE Select	NP_000479.1:p.Val463Phe
NM_001365052.2:c.1243G>T	NP_001351981.1:p.Val415Phe
NM_001386302.1:c.1510G>T	NP_001373231.1:p.Val504Phe
NM_001386303.1:c.1468G>T	NP_001373232.1:p.Val490Phe
NM_001386304.1:c.1366G>T	NP_001373233.1:p.Val456Phe
NM_001386305.1:c.1330G>T	NP_001373234.1:p.Val444Phe
NM_001386306.1:c.1171G>T	NP_001373235.1:p.Val391Phe