Canonical Allele Identifier: CA343772122

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873059T>A (hg19) ; chr1:g.173903921T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903921T>A , CM000663.2:g.173903921T>A	GRCh38
NC_000001.10:g.173873059T>A , CM000663.1:g.173873059T>A	GRCh37
NC_000001.9:g.172139682T>A	NCBI36
NG_012462.1:g.18458A>T , LRG_577:g.18458A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1363A>T MANE Select	ENSP00000356671.3:p.Met455Leu
ENST00000367698.3:c.1363A>T	ENSP00000356671.3:p.Met455Leu
ENST00000617423.4:c.748A>T	ENSP00000478688.1:p.Met250Leu
NM_000488.3:c.1363A>T , LRG_577t1:c.1363A>T	NP_000479.1:p.Met455Leu
XM_005245198.2:c.1219A>T	XP_005245255.1:p.Met407Leu
NM_001365052.1:c.1219A>T	NP_001351981.1:p.Met407Leu
NM_000488.4:c.1363A>T MANE Select	NP_000479.1:p.Met455Leu
NM_001365052.2:c.1219A>T	NP_001351981.1:p.Met407Leu
NM_001386302.1:c.1486A>T	NP_001373231.1:p.Met496Leu
NM_001386303.1:c.1444A>T	NP_001373232.1:p.Met482Leu
NM_001386304.1:c.1342A>T	NP_001373233.1:p.Met448Leu
NM_001386305.1:c.1306A>T	NP_001373234.1:p.Met436Leu
NM_001386306.1:c.1147A>T	NP_001373235.1:p.Met383Leu