Canonical Allele Identifier: CA421821606

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873180T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904042T>G , CM000663.2:g.173904042T>G	GRCh38
NC_000001.10:g.173873180T>G , CM000663.1:g.173873180T>G	GRCh37
NC_000001.9:g.172139803T>G	NCBI36
NG_012462.1:g.18337A>C , LRG_577:g.18337A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1242A>C MANE Select	ENSP00000356671.3:p.Ala414=
ENST00000367698.3:c.1242A>C	ENSP00000356671.3:p.Ala414=
ENST00000617423.4:c.627A>C	ENSP00000478688.1:p.Ala209=
NM_000488.3:c.1242A>C , LRG_577t1:c.1242A>C	NP_000479.1:p.Ala414=
XM_005245198.2:c.1098A>C	XP_005245255.1:p.Ala366=
NM_001365052.1:c.1098A>C	NP_001351981.1:p.Ala366=
NM_000488.4:c.1242A>C MANE Select	NP_000479.1:p.Ala414=
NM_001365052.2:c.1098A>C	NP_001351981.1:p.Ala366=
NM_001386302.1:c.1365A>C	NP_001373231.1:p.Ala455=
NM_001386303.1:c.1323A>C	NP_001373232.1:p.Ala441=
NM_001386304.1:c.1221A>C	NP_001373233.1:p.Ala407=
NM_001386305.1:c.1185A>C	NP_001373234.1:p.Ala395=
NM_001386306.1:c.1026A>C	NP_001373235.1:p.Ala342=