Canonical Allele Identifier: CA343771979

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873028T>G (hg19) ; chr1:g.173903890T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903890T>G , CM000663.2:g.173903890T>G	GRCh38
NC_000001.10:g.173873028T>G , CM000663.1:g.173873028T>G	GRCh37
NC_000001.9:g.172139651T>G	NCBI36
NG_012462.1:g.18489A>C , LRG_577:g.18489A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1394A>C MANE Select	ENSP00000356671.3:p.Ter465Ser
ENST00000367698.3:c.1394A>C	ENSP00000356671.3:p.Ter465Ser
ENST00000617423.4:c.779A>C	ENSP00000478688.1:p.Ter260Ser
NM_000488.3:c.1394A>C , LRG_577t1:c.1394A>C	NP_000479.1:p.Ter465Ser
XM_005245198.2:c.1250A>C	XP_005245255.1:p.Ter417Ser
NM_001365052.1:c.1250A>C	NP_001351981.1:p.Ter417Ser
NM_000488.4:c.1394A>C MANE Select	NP_000479.1:p.Ter465Ser
NM_001365052.2:c.1250A>C	NP_001351981.1:p.Ter417Ser
NM_001386302.1:c.1517A>C	NP_001373231.1:p.Ter506Ser
NM_001386303.1:c.1475A>C	NP_001373232.1:p.Ter492Ser
NM_001386304.1:c.1373A>C	NP_001373233.1:p.Ter458Ser
NM_001386305.1:c.1337A>C	NP_001373234.1:p.Ter446Ser
NM_001386306.1:c.1178A>C	NP_001373235.1:p.Ter393Ser