Canonical Allele Identifier: CA343772453

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873121A>G (hg19) ; chr1:g.173903983A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903983A>G , CM000663.2:g.173903983A>G	GRCh38
NC_000001.10:g.173873121A>G , CM000663.1:g.173873121A>G	GRCh37
NC_000001.9:g.172139744A>G	NCBI36
NG_012462.1:g.18396T>C , LRG_577:g.18396T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1301T>C MANE Select	ENSP00000356671.3:p.Phe434Ser
ENST00000367698.3:c.1301T>C	ENSP00000356671.3:p.Phe434Ser
ENST00000617423.4:c.686T>C	ENSP00000478688.1:p.Phe229Ser
NM_000488.3:c.1301T>C , LRG_577t1:c.1301T>C	NP_000479.1:p.Phe434Ser
XM_005245198.2:c.1157T>C	XP_005245255.1:p.Phe386Ser
NM_001365052.1:c.1157T>C	NP_001351981.1:p.Phe386Ser
NM_000488.4:c.1301T>C MANE Select	NP_000479.1:p.Phe434Ser
NM_001365052.2:c.1157T>C	NP_001351981.1:p.Phe386Ser
NM_001386302.1:c.1424T>C	NP_001373231.1:p.Phe475Ser
NM_001386303.1:c.1382T>C	NP_001373232.1:p.Phe461Ser
NM_001386304.1:c.1280T>C	NP_001373233.1:p.Phe427Ser
NM_001386305.1:c.1244T>C	NP_001373234.1:p.Phe415Ser
NM_001386306.1:c.1085T>C	NP_001373235.1:p.Phe362Ser