Canonical Allele Identifier: CA421821247

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873054G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903916G>A , CM000663.2:g.173903916G>A	GRCh38
NC_000001.10:g.173873054G>A , CM000663.1:g.173873054G>A	GRCh37
NC_000001.9:g.172139677G>A	NCBI36
NG_012462.1:g.18463C>T , LRG_577:g.18463C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1368C>T MANE Select	ENSP00000356671.3:p.Gly456=
ENST00000367698.3:c.1368C>T	ENSP00000356671.3:p.Gly456=
ENST00000617423.4:c.753C>T	ENSP00000478688.1:p.Gly251=
NM_000488.3:c.1368C>T , LRG_577t1:c.1368C>T	NP_000479.1:p.Gly456=
XM_005245198.2:c.1224C>T	XP_005245255.1:p.Gly408=
NM_001365052.1:c.1224C>T	NP_001351981.1:p.Gly408=
NM_000488.4:c.1368C>T MANE Select	NP_000479.1:p.Gly456=
NM_001365052.2:c.1224C>T	NP_001351981.1:p.Gly408=
NM_001386302.1:c.1491C>T	NP_001373231.1:p.Gly497=
NM_001386303.1:c.1449C>T	NP_001373232.1:p.Gly483=
NM_001386304.1:c.1347C>T	NP_001373233.1:p.Gly449=
NM_001386305.1:c.1311C>T	NP_001373234.1:p.Gly437=
NM_001386306.1:c.1152C>T	NP_001373235.1:p.Gly384=