Canonical Allele Identifier: CA2614700360

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047821-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047821A>T , CM000673.2:g.68047821A>T	GRCh38
NC_000011.9:g.67815288A>T , CM000673.1:g.67815288A>T	GRCh37
NC_000011.8:g.67571864A>T	NCBI36
NG_007878.1:g.13806A>T , LRG_115:g.13806A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.88+17A>T
ENST00000698254.1:c.992+17A>T	ENSP00000513629.1:n.992+17A>T
ENST00000698255.1:c.1412+17A>T	ENSP00000513630.1:n.1412+17A>T
ENST00000698256.1:c.929+17A>T
ENST00000698257.1:n.881+17A>T
ENST00000698258.1:n.538A>T
ENST00000698259.1:n.304A>T
ENST00000265686.8:c.1463+17A>T MANE Select	ENSP00000265686.3:n.1463+17A>T
ENST00000265686.7:c.1463+17A>T	ENSP00000265686.3:n.1463+17A>T
ENST00000525516.1:n.257+17A>T
ENST00000525724.5:n.775+17A>T
ENST00000528981.5:c.615+17A>T
ENST00000532635.5:c.815+17A>T	ENSP00000434407.1:n.815+17A>T
ENST00000533005.5:n.516A>T
NM_006019.3:c.1463+17A>T	NP_006010.2:n.1463+17A>T
NM_006053.3:c.815+17A>T	NP_006044.1:n.815+17A>T
XM_005273709.2:c.1463+17A>T	XP_005273766.1:n.1463+17A>T
XM_011544726.1:c.1463+17A>T	XP_011543028.1:n.1463+17A>T
XM_011544727.1:c.1463+17A>T	XP_011543029.1:n.1463+17A>T
XM_011544728.1:c.1463+17A>T	XP_011543030.1:n.1463+17A>T
XM_011544729.1:c.1479+17A>T	XP_011543031.1:n.1479+17A>T
XR_949754.1:n.1467+17A>T
NM_001351059.1:c.569+17A>T	NP_001337988.1:n.569+17A>T
XM_024448320.1:c.1496A>T	XP_024304088.1:p.Gln499Leu
XM_024448321.1:c.1496A>T	XP_024304089.1:p.Gln499Leu
XM_024448322.1:c.1496A>T	XP_024304090.1:p.Gln499Leu
XM_024448323.1:c.1496A>T	XP_024304091.1:p.Gln499Leu
XM_024448324.1:c.1496A>T	XP_024304092.1:p.Gln499Leu
XR_001747721.2:n.1587+17A>T
XR_001747722.1:n.1600+17A>T
XR_001747723.2:n.1600+17A>T
XR_002957115.1:n.1618A>T
NM_006019.4:c.1463+17A>T MANE Select	NP_006010.2:n.1463+17A>T
NM_001351059.2:c.569+17A>T	NP_001337988.1:n.569+17A>T
NM_006053.4:c.815+17A>T	NP_006044.1:n.815+17A>T