Canonical Allele Identifier: CA381579623

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043909T>G , CM000673.2:g.68043909T>G	GRCh38
NC_000011.9:g.67811376T>G , CM000673.1:g.67811376T>G	GRCh37
NC_000011.8:g.67567952T>G	NCBI36
NG_007878.1:g.9894T>G , LRG_115:g.9894T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.807+2T>G MANE Select	NP_006010.2:n.807+2T>G
ENST00000265686.8:c.807+2T>G MANE Select	ENSP00000265686.3:n.807+2T>G
NM_001351059.1:c.-88+2T>G	NP_001337988.1:n.-88+2T>G
NM_001351059.2:c.-88+2T>G	NP_001337988.1:n.-88+2T>G
NM_006019.3:c.807+2T>G	NP_006010.2:n.807+2T>G
NM_006053.3:c.159+2T>G	NP_006044.1:n.159+2T>G
NM_006053.4:c.159+2T>G	NP_006044.1:n.159+2T>G
ENST00000265686.7:c.807+2T>G	ENSP00000265686.3:n.807+2T>G
ENST00000524598.5:c.765+2T>G	ENSP00000432846.1:n.765+2T>G
ENST00000525724.5:n.119+2T>G
ENST00000527530.1:n.425+2T>G
ENST00000529364.1:c.307+2T>G
ENST00000532635.5:c.159+2T>G	ENSP00000434407.1:n.159+2T>G
ENST00000534673.5:c.*155+2T>G	ENSP00000431174.1:n.*155+2T>G
ENST00000698254.1:c.404-290T>G	ENSP00000513629.1:n.404-290T>G
ENST00000698255.1:c.756+2T>G	ENSP00000513630.1:n.756+2T>G
ENST00000698256.1:c.273+2T>G
ENST00000698257.1:n.225+2T>G
XM_005273709.2:c.807+2T>G	XP_005273766.1:n.807+2T>G
XM_011544726.1:c.807+2T>G	XP_011543028.1:n.807+2T>G
XM_011544727.1:c.807+2T>G	XP_011543029.1:n.807+2T>G
XM_011544728.1:c.807+2T>G	XP_011543030.1:n.807+2T>G
XM_011544729.1:c.823+2T>G	XP_011543031.1:n.823+2T>G
XM_024448320.1:c.823+2T>G	XP_024304088.1:n.823+2T>G
XM_024448321.1:c.823+2T>G	XP_024304089.1:n.823+2T>G
XM_024448322.1:c.823+2T>G	XP_024304090.1:n.823+2T>G
XM_024448323.1:c.823+2T>G	XP_024304091.1:n.823+2T>G
XM_024448324.1:c.823+2T>G	XP_024304092.1:n.823+2T>G
XR_001747721.2:n.931+2T>G
XR_001747722.1:n.944+2T>G
XR_001747723.2:n.944+2T>G
XR_002957115.1:n.945+2T>G
XR_949754.1:n.811+2T>G