Canonical Allele Identifier: CA343774120

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878891G>A (hg19) ; chr1:g.173909753G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909753G>A , CM000663.2:g.173909753G>A	GRCh38
NC_000001.10:g.173878891G>A , CM000663.1:g.173878891G>A	GRCh37
NC_000001.9:g.172145514G>A	NCBI36
NG_012462.1:g.12626C>T , LRG_577:g.12626C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.952C>T MANE Select	ENSP00000356671.3:p.Pro318Ser
ENST00000367698.3:c.952C>T	ENSP00000356671.3:p.Pro318Ser
ENST00000487183.1:n.603C>T
ENST00000617423.4:c.559+2111C>T	ENSP00000478688.1:n.559+2111C>T
NM_000488.3:c.952C>T , LRG_577t1:c.952C>T	NP_000479.1:p.Pro318Ser
XM_005245198.2:c.808C>T	XP_005245255.1:p.Pro270Ser
NM_001365052.1:c.808C>T	NP_001351981.1:p.Pro270Ser
NM_000488.4:c.952C>T MANE Select	NP_000479.1:p.Pro318Ser
NM_001365052.2:c.808C>T	NP_001351981.1:p.Pro270Ser
NM_001386302.1:c.1075C>T	NP_001373231.1:p.Pro359Ser
NM_001386303.1:c.1033C>T	NP_001373232.1:p.Pro345Ser
NM_001386304.1:c.931C>T	NP_001373233.1:p.Pro311Ser
NM_001386305.1:c.895C>T	NP_001373234.1:p.Pro299Ser
NM_001386306.1:c.736C>T	NP_001373235.1:p.Pro246Ser