Canonical Allele Identifier: CA421942932

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878844T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909706T>G , CM000663.2:g.173909706T>G	GRCh38
NC_000001.10:g.173878844T>G , CM000663.1:g.173878844T>G	GRCh37
NC_000001.9:g.172145467T>G	NCBI36
NG_012462.1:g.12673A>C , LRG_577:g.12673A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.999A>C MANE Select	ENSP00000356671.3:p.Pro333=
ENST00000367698.3:c.999A>C	ENSP00000356671.3:p.Pro333=
ENST00000617423.4:c.559+2158A>C	ENSP00000478688.1:n.559+2158A>C
NM_000488.3:c.999A>C , LRG_577t1:c.999A>C	NP_000479.1:p.Pro333=
XM_005245198.2:c.855A>C	XP_005245255.1:p.Pro285=
NM_001365052.1:c.855A>C	NP_001351981.1:p.Pro285=
NM_000488.4:c.999A>C MANE Select	NP_000479.1:p.Pro333=
NM_001365052.2:c.855A>C	NP_001351981.1:p.Pro285=
NM_001386302.1:c.1122A>C	NP_001373231.1:p.Pro374=
NM_001386303.1:c.1080A>C	NP_001373232.1:p.Pro360=
NM_001386304.1:c.978A>C	NP_001373233.1:p.Pro326=
NM_001386305.1:c.942A>C	NP_001373234.1:p.Pro314=
NM_001386306.1:c.783A>C	NP_001373235.1:p.Pro261=