Canonical Allele Identifier: CA381579614

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043908G>A , CM000673.2:g.68043908G>A	GRCh38
NC_000011.9:g.67811375G>A , CM000673.1:g.67811375G>A	GRCh37
NC_000011.8:g.67567951G>A	NCBI36
NG_007878.1:g.9893G>A , LRG_115:g.9893G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.807+1G>A MANE Select	NP_006010.2:n.807+1G>A
ENST00000265686.8:c.807+1G>A MANE Select	ENSP00000265686.3:n.807+1G>A
NM_001351059.1:c.-88+1G>A	NP_001337988.1:n.-88+1G>A
NM_001351059.2:c.-88+1G>A	NP_001337988.1:n.-88+1G>A
NM_006019.3:c.807+1G>A	NP_006010.2:n.807+1G>A
NM_006053.3:c.159+1G>A	NP_006044.1:n.159+1G>A
NM_006053.4:c.159+1G>A	NP_006044.1:n.159+1G>A
ENST00000265686.7:c.807+1G>A	ENSP00000265686.3:n.807+1G>A
ENST00000524598.5:c.765+1G>A	ENSP00000432846.1:n.765+1G>A
ENST00000525724.5:n.119+1G>A
ENST00000527530.1:n.425+1G>A
ENST00000529364.1:c.307+1G>A
ENST00000532635.5:c.159+1G>A	ENSP00000434407.1:n.159+1G>A
ENST00000534673.5:c.*155+1G>A	ENSP00000431174.1:n.*155+1G>A
ENST00000698254.1:c.404-291G>A	ENSP00000513629.1:n.404-291G>A
ENST00000698255.1:c.756+1G>A	ENSP00000513630.1:n.756+1G>A
ENST00000698256.1:c.273+1G>A
ENST00000698257.1:n.225+1G>A
XM_005273709.2:c.807+1G>A	XP_005273766.1:n.807+1G>A
XM_011544726.1:c.807+1G>A	XP_011543028.1:n.807+1G>A
XM_011544727.1:c.807+1G>A	XP_011543029.1:n.807+1G>A
XM_011544728.1:c.807+1G>A	XP_011543030.1:n.807+1G>A
XM_011544729.1:c.823+1G>A	XP_011543031.1:n.823+1G>A
XM_024448320.1:c.823+1G>A	XP_024304088.1:n.823+1G>A
XM_024448321.1:c.823+1G>A	XP_024304089.1:n.823+1G>A
XM_024448322.1:c.823+1G>A	XP_024304090.1:n.823+1G>A
XM_024448323.1:c.823+1G>A	XP_024304091.1:n.823+1G>A
XM_024448324.1:c.823+1G>A	XP_024304092.1:n.823+1G>A
XR_001747721.2:n.931+1G>A
XR_001747722.1:n.944+1G>A
XR_001747723.2:n.944+1G>A
XR_002957115.1:n.945+1G>A
XR_949754.1:n.811+1G>A