Canonical Allele Identifier: CA421942928

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878838C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909700C>A , CM000663.2:g.173909700C>A	GRCh38
NC_000001.10:g.173878838C>A , CM000663.1:g.173878838C>A	GRCh37
NC_000001.9:g.172145461C>A	NCBI36
NG_012462.1:g.12679G>T , LRG_577:g.12679G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1005G>T MANE Select	ENSP00000356671.3:p.Val335=
ENST00000367698.3:c.1005G>T	ENSP00000356671.3:p.Val335=
ENST00000617423.4:c.559+2164G>T	ENSP00000478688.1:n.559+2164G>T
NM_000488.3:c.1005G>T , LRG_577t1:c.1005G>T	NP_000479.1:p.Val335=
XM_005245198.2:c.861G>T	XP_005245255.1:p.Val287=
NM_001365052.1:c.861G>T	NP_001351981.1:p.Val287=
NM_000488.4:c.1005G>T MANE Select	NP_000479.1:p.Val335=
NM_001365052.2:c.861G>T	NP_001351981.1:p.Val287=
NM_001386302.1:c.1128G>T	NP_001373231.1:p.Val376=
NM_001386303.1:c.1086G>T	NP_001373232.1:p.Val362=
NM_001386304.1:c.984G>T	NP_001373233.1:p.Val328=
NM_001386305.1:c.948G>T	NP_001373234.1:p.Val316=
NM_001386306.1:c.789G>T	NP_001373235.1:p.Val263=