Canonical Allele Identifier: CA343772331

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1188571702
• MyVariant Identifiers: chr1:g.173873100A>G (hg19) ; chr1:g.173903962A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903962A>G , CM000663.2:g.173903962A>G	GRCh38
NC_000001.10:g.173873100A>G , CM000663.1:g.173873100A>G	GRCh37
NC_000001.9:g.172139723A>G	NCBI36
NG_012462.1:g.18417T>C , LRG_577:g.18417T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1322T>C MANE Select	ENSP00000356671.3:p.Leu441Pro
ENST00000367698.3:c.1322T>C	ENSP00000356671.3:p.Leu441Pro
ENST00000617423.4:c.707T>C	ENSP00000478688.1:p.Leu236Pro
NM_000488.3:c.1322T>C , LRG_577t1:c.1322T>C	NP_000479.1:p.Leu441Pro
XM_005245198.2:c.1178T>C	XP_005245255.1:p.Leu393Pro
NM_001365052.1:c.1178T>C	NP_001351981.1:p.Leu393Pro
NM_000488.4:c.1322T>C MANE Select	NP_000479.1:p.Leu441Pro
NM_001365052.2:c.1178T>C	NP_001351981.1:p.Leu393Pro
NM_001386302.1:c.1445T>C	NP_001373231.1:p.Leu482Pro
NM_001386303.1:c.1403T>C	NP_001373232.1:p.Leu468Pro
NM_001386304.1:c.1301T>C	NP_001373233.1:p.Leu434Pro
NM_001386305.1:c.1265T>C	NP_001373234.1:p.Leu422Pro
NM_001386306.1:c.1106T>C	NP_001373235.1:p.Leu369Pro