Canonical Allele Identifier: CA33679981

Gene: TOR1AIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179901389G>A , CM000663.2:g.179901389G>A	GRCh38
NC_000001.10:g.179870524G>A , CM000663.1:g.179870524G>A	GRCh37
NC_000001.9:g.178137147G>A	NCBI36
NG_042316.1:g.24348G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015602.4:c.739+1G>A MANE Select	NP_056417.2:n.739+1G>A
ENST00000606911.7:c.739+1G>A MANE Select	ENSP00000476687.1:n.739+1G>A
NM_001267578.1:c.742+1G>A	NP_001254507.1:n.742+1G>A
NM_001267578.2:c.742+1G>A	NP_001254507.1:n.742+1G>A
NM_015602.3:c.739+1G>A	NP_056417.2:n.739+1G>A
ENST00000271583.7:c.742+1G>A	ENSP00000271583.3:n.742+1G>A
ENST00000435319.8:c.376+1G>A	ENSP00000393292.3:n.376+1G>A
ENST00000474875.5:n.331+1G>A
ENST00000524653.1:n.308+1G>A
ENST00000527391.5:c.368+1G>A
ENST00000528443.6:c.742+1G>A	ENSP00000435365.2:n.742+1G>A
ENST00000529091.5:c.530+1G>A
ENST00000531630.6:c.406+1G>A	ENSP00000434316.2:n.406+1G>A
ENST00000531726.5:n.328+1G>A
ENST00000606911.6:c.739+1G>A	ENSP00000476687.1:n.739+1G>A
XM_011509403.1:c.742+1G>A	XP_011507705.1:n.742+1G>A
XM_011509403.2:c.742+1G>A	XP_011507705.1:n.742+1G>A
XM_011509404.1:c.739+1G>A	XP_011507706.1:n.739+1G>A
XM_011509404.2:c.739+1G>A	XP_011507706.1:n.739+1G>A
XM_024446305.1:c.-162+1G>A	XP_024302073.1:n.-162+1G>A