Canonical Allele Identifier: CA343772421

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873116C>G (hg19) ; chr1:g.173903978C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903978C>G , CM000663.2:g.173903978C>G	GRCh38
NC_000001.10:g.173873116C>G , CM000663.1:g.173873116C>G	GRCh37
NC_000001.9:g.172139739C>G	NCBI36
NG_012462.1:g.18401G>C , LRG_577:g.18401G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1306G>C MANE Select	ENSP00000356671.3:p.Ala436Pro
ENST00000367698.3:c.1306G>C	ENSP00000356671.3:p.Ala436Pro
ENST00000617423.4:c.691G>C	ENSP00000478688.1:p.Ala231Pro
NM_000488.3:c.1306G>C , LRG_577t1:c.1306G>C	NP_000479.1:p.Ala436Pro
XM_005245198.2:c.1162G>C	XP_005245255.1:p.Ala388Pro
NM_001365052.1:c.1162G>C	NP_001351981.1:p.Ala388Pro
NM_000488.4:c.1306G>C MANE Select	NP_000479.1:p.Ala436Pro
NM_001365052.2:c.1162G>C	NP_001351981.1:p.Ala388Pro
NM_001386302.1:c.1429G>C	NP_001373231.1:p.Ala477Pro
NM_001386303.1:c.1387G>C	NP_001373232.1:p.Ala463Pro
NM_001386304.1:c.1285G>C	NP_001373233.1:p.Ala429Pro
NM_001386305.1:c.1249G>C	NP_001373234.1:p.Ala417Pro
NM_001386306.1:c.1090G>C	NP_001373235.1:p.Ala364Pro