Canonical Allele Identifier: CA2614699346

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047592-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047592T>C , CM000673.2:g.68047592T>C	GRCh38
NC_000011.9:g.67815059T>C , CM000673.1:g.67815059T>C	GRCh37
NC_000011.8:g.67571635T>C	NCBI36
NG_007878.1:g.13577T>C , LRG_115:g.13577T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.834+20T>C	ENSP00000513629.1:n.834+20T>C
ENST00000698255.1:c.1254+20T>C	ENSP00000513630.1:n.1254+20T>C
ENST00000698256.1:c.771+20T>C
ENST00000698257.1:n.723+20T>C
ENST00000698258.1:n.309T>C
ENST00000698259.1:n.129+20T>C
ENST00000265686.8:c.1305+20T>C MANE Select	ENSP00000265686.3:n.1305+20T>C
ENST00000265686.7:c.1305+20T>C	ENSP00000265686.3:n.1305+20T>C
ENST00000525516.1:n.99+20T>C
ENST00000525724.5:n.617+20T>C
ENST00000528981.5:c.457+20T>C
ENST00000529364.1:c.716+20T>C
ENST00000532635.5:c.657+20T>C	ENSP00000434407.1:n.657+20T>C
ENST00000533005.5:n.341+20T>C
NM_006019.3:c.1305+20T>C	NP_006010.2:n.1305+20T>C
NM_006053.3:c.657+20T>C	NP_006044.1:n.657+20T>C
XM_005273709.2:c.1305+20T>C	XP_005273766.1:n.1305+20T>C
XM_011544726.1:c.1305+20T>C	XP_011543028.1:n.1305+20T>C
XM_011544727.1:c.1305+20T>C	XP_011543029.1:n.1305+20T>C
XM_011544728.1:c.1305+20T>C	XP_011543030.1:n.1305+20T>C
XM_011544729.1:c.1321+20T>C	XP_011543031.1:n.1321+20T>C
XR_949754.1:n.1309+20T>C
NM_001351059.1:c.411+20T>C	NP_001337988.1:n.411+20T>C
XM_024448320.1:c.1321+20T>C	XP_024304088.1:n.1321+20T>C
XM_024448321.1:c.1321+20T>C	XP_024304089.1:n.1321+20T>C
XM_024448322.1:c.1321+20T>C	XP_024304090.1:n.1321+20T>C
XM_024448323.1:c.1321+20T>C	XP_024304091.1:n.1321+20T>C
XM_024448324.1:c.1321+20T>C	XP_024304092.1:n.1321+20T>C
XR_001747721.2:n.1429+20T>C
XR_001747722.1:n.1442+20T>C
XR_001747723.2:n.1442+20T>C
XR_002957115.1:n.1443+20T>C
NM_006019.4:c.1305+20T>C MANE Select	NP_006010.2:n.1305+20T>C
NM_001351059.2:c.411+20T>C	NP_001337988.1:n.411+20T>C
NM_006053.4:c.657+20T>C	NP_006044.1:n.657+20T>C