Canonical Allele Identifier: CA1269024

Gene: TOR1AIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179908674G>A , CM000663.2:g.179908674G>A	GRCh38
NC_000001.10:g.179877809G>A , CM000663.1:g.179877809G>A	GRCh37
NC_000001.9:g.178144432G>A	NCBI36
NG_042316.1:g.31633G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015602.4:c.907+1G>A MANE Select	NP_056417.2:n.907+1G>A
ENST00000606911.7:c.907+1G>A MANE Select	ENSP00000476687.1:n.907+1G>A
NM_001267578.1:c.910+1G>A	NP_001254507.1:n.910+1G>A
NM_001267578.2:c.910+1G>A	NP_001254507.1:n.910+1G>A
NM_015602.3:c.907+1G>A	NP_056417.2:n.907+1G>A
ENST00000271583.7:c.910+1G>A	ENSP00000271583.3:n.910+1G>A
ENST00000435319.8:c.544+1G>A	ENSP00000393292.3:n.544+1G>A
ENST00000447964.1:c.168+1G>A
ENST00000474875.5:n.499+1G>A
ENST00000527391.5:c.536+1G>A
ENST00000528443.6:c.910+1G>A	ENSP00000435365.2:n.910+1G>A
ENST00000531630.6:c.574+1G>A	ENSP00000434316.2:n.574+1G>A
ENST00000606911.6:c.907+1G>A	ENSP00000476687.1:n.907+1G>A
XM_011509403.1:c.910+1G>A	XP_011507705.1:n.910+1G>A
XM_011509403.2:c.910+1G>A	XP_011507705.1:n.910+1G>A
XM_011509404.1:c.907+1G>A	XP_011507706.1:n.907+1G>A
XM_011509404.2:c.907+1G>A	XP_011507706.1:n.907+1G>A
XM_024446305.1:c.7+1G>A	XP_024302073.1:n.7+1G>A