Canonical Allele Identifier: CA421942779

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878697T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909559T>C , CM000663.2:g.173909559T>C	GRCh38
NC_000001.10:g.173878697T>C , CM000663.1:g.173878697T>C	GRCh37
NC_000001.9:g.172145320T>C	NCBI36
NG_012462.1:g.12820A>G , LRG_577:g.12820A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1146A>G MANE Select	ENSP00000356671.3:p.Lys382=
ENST00000367698.3:c.1146A>G	ENSP00000356671.3:p.Lys382=
ENST00000617423.4:c.560-2066A>G	ENSP00000478688.1:n.560-2066A>G
NM_000488.3:c.1146A>G , LRG_577t1:c.1146A>G	NP_000479.1:p.Lys382=
XM_005245198.2:c.1002A>G	XP_005245255.1:p.Lys334=
NM_001365052.1:c.1002A>G	NP_001351981.1:p.Lys334=
NM_000488.4:c.1146A>G MANE Select	NP_000479.1:p.Lys382=
NM_001365052.2:c.1002A>G	NP_001351981.1:p.Lys334=
NM_001386302.1:c.1269A>G	NP_001373231.1:p.Lys423=
NM_001386303.1:c.1227A>G	NP_001373232.1:p.Lys409=
NM_001386304.1:c.1125A>G	NP_001373233.1:p.Lys375=
NM_001386305.1:c.1089A>G	NP_001373234.1:p.Lys363=
NM_001386306.1:c.930A>G	NP_001373235.1:p.Lys310=