Canonical Allele Identifier: CA343777159

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173883689A>T (hg19) ; chr1:g.173914551A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914551A>T , CM000663.2:g.173914551A>T	GRCh38
NC_000001.10:g.173883689A>T , CM000663.1:g.173883689A>T	GRCh37
NC_000001.9:g.172150312A>T	NCBI36
NG_012462.1:g.7828T>A , LRG_577:g.7828T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.408+2T>A MANE Select	ENSP00000356671.3:n.408+2T>A
ENST00000367698.3:c.408+2T>A	ENSP00000356671.3:n.408+2T>A
ENST00000487183.1:n.113+2T>A
ENST00000494024.1:n.634+2T>A
ENST00000617423.4:c.408+2T>A	ENSP00000478688.1:n.408+2T>A
NM_000488.3:c.408+2T>A , LRG_577t1:c.408+2T>A	NP_000479.1:n.408+2T>A
XM_005245198.2:c.264+2T>A	XP_005245255.1:n.264+2T>A
NM_001365052.1:c.264+2T>A	NP_001351981.1:n.264+2T>A
NM_000488.4:c.408+2T>A MANE Select	NP_000479.1:n.408+2T>A
NM_001365052.2:c.264+2T>A	NP_001351981.1:n.264+2T>A
NM_001386302.1:c.408+2T>A	NP_001373231.1:n.408+2T>A
NM_001386303.1:c.489+2T>A	NP_001373232.1:n.489+2T>A
NM_001386304.1:c.408+2T>A	NP_001373233.1:n.408+2T>A
NM_001386305.1:c.408+2T>A	NP_001373234.1:n.408+2T>A
NM_001386306.1:c.408+2T>A	NP_001373235.1:n.408+2T>A