Canonical Allele Identifier: CA2614699457

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047628-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047628C>A , CM000673.2:g.68047628C>A	GRCh38
NC_000011.9:g.67815095C>A , CM000673.1:g.67815095C>A	GRCh37
NC_000011.8:g.67571671C>A	NCBI36
NG_007878.1:g.13613C>A , LRG_115:g.13613C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.835-19C>A	ENSP00000513629.1:n.835-19C>A
ENST00000698255.1:c.1255-19C>A	ENSP00000513630.1:n.1255-19C>A
ENST00000698256.1:c.772-19C>A
ENST00000698257.1:n.724-19C>A
ENST00000698258.1:n.345C>A
ENST00000698259.1:n.130-19C>A
ENST00000265686.8:c.1306-19C>A MANE Select	ENSP00000265686.3:n.1306-19C>A
ENST00000265686.7:c.1306-19C>A	ENSP00000265686.3:n.1306-19C>A
ENST00000525516.1:n.100-19C>A
ENST00000525724.5:n.618-19C>A
ENST00000528981.5:c.458-19C>A
ENST00000529364.1:c.717-19C>A
ENST00000532635.5:c.658-19C>A	ENSP00000434407.1:n.658-19C>A
ENST00000533005.5:n.342-19C>A
NM_006019.3:c.1306-19C>A	NP_006010.2:n.1306-19C>A
NM_006053.3:c.658-19C>A	NP_006044.1:n.658-19C>A
XM_005273709.2:c.1306-19C>A	XP_005273766.1:n.1306-19C>A
XM_011544726.1:c.1306-19C>A	XP_011543028.1:n.1306-19C>A
XM_011544727.1:c.1306-19C>A	XP_011543029.1:n.1306-19C>A
XM_011544728.1:c.1306-19C>A	XP_011543030.1:n.1306-19C>A
XM_011544729.1:c.1322-19C>A	XP_011543031.1:n.1322-19C>A
XR_949754.1:n.1310-19C>A
NM_001351059.1:c.412-19C>A	NP_001337988.1:n.412-19C>A
XM_024448320.1:c.1322-19C>A	XP_024304088.1:n.1322-19C>A
XM_024448321.1:c.1322-19C>A	XP_024304089.1:n.1322-19C>A
XM_024448322.1:c.1322-19C>A	XP_024304090.1:n.1322-19C>A
XM_024448323.1:c.1322-19C>A	XP_024304091.1:n.1322-19C>A
XM_024448324.1:c.1322-19C>A	XP_024304092.1:n.1322-19C>A
XR_001747721.2:n.1430-19C>A
XR_001747722.1:n.1443-19C>A
XR_001747723.2:n.1443-19C>A
XR_002957115.1:n.1444-19C>A
NM_006019.4:c.1306-19C>A MANE Select	NP_006010.2:n.1306-19C>A
NM_001351059.2:c.412-19C>A	NP_001337988.1:n.412-19C>A
NM_006053.4:c.658-19C>A	NP_006044.1:n.658-19C>A