Canonical Allele Identifier: CA343776846

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173881137T>A (hg19) ; chr1:g.173911999T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911999T>A , CM000663.2:g.173911999T>A	GRCh38
NC_000001.10:g.173881137T>A , CM000663.1:g.173881137T>A	GRCh37
NC_000001.9:g.172147760T>A	NCBI36
NG_012462.1:g.10380A>T , LRG_577:g.10380A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.424A>T MANE Select	ENSP00000356671.3:p.Thr142Ser
ENST00000367698.3:c.424A>T	ENSP00000356671.3:p.Thr142Ser
ENST00000487183.1:n.129A>T
ENST00000494024.1:n.650A>T
ENST00000617423.4:c.424A>T	ENSP00000478688.1:p.Thr142Ser
NM_000488.3:c.424A>T , LRG_577t1:c.424A>T	NP_000479.1:p.Thr142Ser
XM_005245198.2:c.280A>T	XP_005245255.1:p.Thr94Ser
NM_001365052.1:c.280A>T	NP_001351981.1:p.Thr94Ser
NM_000488.4:c.424A>T MANE Select	NP_000479.1:p.Thr142Ser
NM_001365052.2:c.280A>T	NP_001351981.1:p.Thr94Ser
NM_001386302.1:c.424A>T	NP_001373231.1:p.Thr142Ser
NM_001386303.1:c.505A>T	NP_001373232.1:p.Thr169Ser
NM_001386304.1:c.424A>T	NP_001373233.1:p.Thr142Ser
NM_001386305.1:c.424A>T	NP_001373234.1:p.Thr142Ser
NM_001386306.1:c.409-1108A>T	NP_001373235.1:n.409-1108A>T