Canonical Allele Identifier: CA343774089

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1657685129
• MyVariant Identifiers: chr1:g.173878884G>A (hg19) ; chr1:g.173909746G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909746G>A , CM000663.2:g.173909746G>A	GRCh38
NC_000001.10:g.173878884G>A , CM000663.1:g.173878884G>A	GRCh37
NC_000001.9:g.172145507G>A	NCBI36
NG_012462.1:g.12633C>T , LRG_577:g.12633C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.959C>T MANE Select	ENSP00000356671.3:p.Pro320Leu
ENST00000367698.3:c.959C>T	ENSP00000356671.3:p.Pro320Leu
ENST00000487183.1:n.610C>T
ENST00000617423.4:c.559+2118C>T	ENSP00000478688.1:n.559+2118C>T
NM_000488.3:c.959C>T , LRG_577t1:c.959C>T	NP_000479.1:p.Pro320Leu
XM_005245198.2:c.815C>T	XP_005245255.1:p.Pro272Leu
NM_001365052.1:c.815C>T	NP_001351981.1:p.Pro272Leu
NM_000488.4:c.959C>T MANE Select	NP_000479.1:p.Pro320Leu
NM_001365052.2:c.815C>T	NP_001351981.1:p.Pro272Leu
NM_001386302.1:c.1082C>T	NP_001373231.1:p.Pro361Leu
NM_001386303.1:c.1040C>T	NP_001373232.1:p.Pro347Leu
NM_001386304.1:c.938C>T	NP_001373233.1:p.Pro313Leu
NM_001386305.1:c.902C>T	NP_001373234.1:p.Pro301Leu
NM_001386306.1:c.743C>T	NP_001373235.1:p.Pro248Leu