Canonical Allele Identifier: CA224210002

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68049425G>A , CM000673.2:g.68049425G>A	GRCh38
NC_000011.9:g.67816892G>A , CM000673.1:g.67816892G>A	GRCh37
NC_000011.8:g.67573468G>A	NCBI36
NG_007878.1:g.15410G>A , LRG_115:g.15410G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1887+131G>A MANE Select	NP_006010.2:n.1887+131G>A
ENST00000265686.8:c.1887+131G>A MANE Select	ENSP00000265686.3:n.1887+131G>A
NM_001351059.1:c.993+131G>A	NP_001337988.1:n.993+131G>A
NM_001351059.2:c.993+131G>A	NP_001337988.1:n.993+131G>A
NM_006019.3:c.1887+131G>A	NP_006010.2:n.1887+131G>A
NM_006053.3:c.1239+131G>A	NP_006044.1:n.1239+131G>A
NM_006053.4:c.1239+131G>A	NP_006044.1:n.1239+131G>A
ENST00000265686.7:c.1887+131G>A	ENSP00000265686.3:n.1887+131G>A
ENST00000524870.1:n.278G>A
ENST00000525724.5:n.1199+131G>A
ENST00000530449.2:n.643G>A
ENST00000532635.5:c.1239+131G>A	ENSP00000434407.1:n.1239+131G>A
ENST00000533005.5:n.1000+131G>A
ENST00000698254.1:c.1416+131G>A	ENSP00000513629.1:n.1416+131G>A
ENST00000698255.1:c.1836+131G>A	ENSP00000513630.1:n.1836+131G>A
ENST00000698256.1:c.1353+131G>A
ENST00000698257.1:n.1305+131G>A
ENST00000698258.1:n.1022+131G>A
ENST00000698259.1:n.919G>A
XM_005273709.2:c.1887+131G>A	XP_005273766.1:n.1887+131G>A
XM_011544726.1:c.1887+131G>A	XP_011543028.1:n.1887+131G>A
XM_011544727.1:c.1887+131G>A	XP_011543029.1:n.1887+131G>A
XM_011544728.1:c.1887+131G>A	XP_011543030.1:n.1887+131G>A
XM_024448320.1:c.1980+131G>A	XP_024304088.1:n.1980+131G>A
XM_024448321.1:c.1980+131G>A	XP_024304089.1:n.1980+131G>A
XM_024448322.1:c.1980+131G>A	XP_024304090.1:n.1980+131G>A
XM_024448323.1:c.1980+131G>A	XP_024304091.1:n.1980+131G>A
XM_024448324.1:c.1980+131G>A	XP_024304092.1:n.1980+131G>A
XR_001747721.2:n.2011+131G>A
XR_001747722.1:n.2024+131G>A
XR_001747723.2:n.2024+131G>A
XR_002957115.1:n.2233G>A
XR_949754.1:n.2022G>A