Canonical Allele Identifier: CA343772437

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873118T>G (hg19) ; chr1:g.173903980T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903980T>G , CM000663.2:g.173903980T>G	GRCh38
NC_000001.10:g.173873118T>G , CM000663.1:g.173873118T>G	GRCh37
NC_000001.9:g.172139741T>G	NCBI36
NG_012462.1:g.18399A>C , LRG_577:g.18399A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1304A>C MANE Select	ENSP00000356671.3:p.Lys435Thr
ENST00000367698.3:c.1304A>C	ENSP00000356671.3:p.Lys435Thr
ENST00000617423.4:c.689A>C	ENSP00000478688.1:p.Lys230Thr
NM_000488.3:c.1304A>C , LRG_577t1:c.1304A>C	NP_000479.1:p.Lys435Thr
XM_005245198.2:c.1160A>C	XP_005245255.1:p.Lys387Thr
NM_001365052.1:c.1160A>C	NP_001351981.1:p.Lys387Thr
NM_000488.4:c.1304A>C MANE Select	NP_000479.1:p.Lys435Thr
NM_001365052.2:c.1160A>C	NP_001351981.1:p.Lys387Thr
NM_001386302.1:c.1427A>C	NP_001373231.1:p.Lys476Thr
NM_001386303.1:c.1385A>C	NP_001373232.1:p.Lys462Thr
NM_001386304.1:c.1283A>C	NP_001373233.1:p.Lys428Thr
NM_001386305.1:c.1247A>C	NP_001373234.1:p.Lys416Thr
NM_001386306.1:c.1088A>C	NP_001373235.1:p.Lys363Thr