Canonical Allele Identifier: CA421821338

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873081A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903943A>G , CM000663.2:g.173903943A>G	GRCh38
NC_000001.10:g.173873081A>G , CM000663.1:g.173873081A>G	GRCh37
NC_000001.9:g.172139704A>G	NCBI36
NG_012462.1:g.18436T>C , LRG_577:g.18436T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1341T>C MANE Select	ENSP00000356671.3:p.Val447=
ENST00000367698.3:c.1341T>C	ENSP00000356671.3:p.Val447=
ENST00000617423.4:c.726T>C	ENSP00000478688.1:p.Val242=
NM_000488.3:c.1341T>C , LRG_577t1:c.1341T>C	NP_000479.1:p.Val447=
XM_005245198.2:c.1197T>C	XP_005245255.1:p.Val399=
NM_001365052.1:c.1197T>C	NP_001351981.1:p.Val399=
NM_000488.4:c.1341T>C MANE Select	NP_000479.1:p.Val447=
NM_001365052.2:c.1197T>C	NP_001351981.1:p.Val399=
NM_001386302.1:c.1464T>C	NP_001373231.1:p.Val488=
NM_001386303.1:c.1422T>C	NP_001373232.1:p.Val474=
NM_001386304.1:c.1320T>C	NP_001373233.1:p.Val440=
NM_001386305.1:c.1284T>C	NP_001373234.1:p.Val428=
NM_001386306.1:c.1125T>C	NP_001373235.1:p.Val375=