Canonical Allele Identifier: CA381588663

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68049662G>T , CM000673.2:g.68049662G>T	GRCh38
NC_000011.9:g.67817129G>T , CM000673.1:g.67817129G>T	GRCh37
NC_000011.8:g.67573705G>T	NCBI36
NG_007878.1:g.15647G>T , LRG_115:g.15647G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1888-1G>T MANE Select	NP_006010.2:n.1888-1G>T
ENST00000265686.8:c.1888-1G>T MANE Select	ENSP00000265686.3:n.1888-1G>T
NM_001351059.1:c.994-1G>T	NP_001337988.1:n.994-1G>T
NM_001351059.2:c.994-1G>T	NP_001337988.1:n.994-1G>T
NM_006019.3:c.1888-1G>T	NP_006010.2:n.1888-1G>T
NM_006053.3:c.1240-1G>T	NP_006044.1:n.1240-1G>T
NM_006053.4:c.1240-1G>T	NP_006044.1:n.1240-1G>T
ENST00000265686.7:c.1888-1G>T	ENSP00000265686.3:n.1888-1G>T
ENST00000524870.1:n.515G>T
ENST00000525724.5:n.1200-1G>T
ENST00000530449.2:n.880G>T
ENST00000532635.5:c.1240-1G>T	ENSP00000434407.1:n.1240-1G>T
ENST00000533005.5:n.1001-1G>T
ENST00000698254.1:c.1417-1G>T	ENSP00000513629.1:n.1417-1G>T
ENST00000698255.1:c.1837-1G>T	ENSP00000513630.1:n.1837-1G>T
ENST00000698256.1:c.1354-1G>T
ENST00000698257.1:n.1306-1G>T
ENST00000698258.1:n.1023-1G>T
ENST00000698259.1:n.1156G>T
XM_005273709.2:c.1888-1G>T	XP_005273766.1:n.1888-1G>T
XM_011544726.1:c.1888-1G>T	XP_011543028.1:n.1888-1G>T
XM_011544727.1:c.1888-1G>T	XP_011543029.1:n.1888-1G>T
XM_024448320.1:c.1981-1G>T	XP_024304088.1:n.1981-1G>T
XM_024448321.1:c.1981-1G>T	XP_024304089.1:n.1981-1G>T
XM_024448322.1:c.1981-1G>T	XP_024304090.1:n.1981-1G>T
XM_024448323.1:c.1981-1G>T	XP_024304091.1:n.1981-1G>T
XM_024448324.1:c.*21G>T	XP_024304092.1:n.*21G>T
XR_001747721.2:n.2056G>T
XR_001747722.1:n.2025-1G>T
XR_001747723.2:n.2069G>T
XR_002957115.1:n.2246-1G>T
XR_949754.1:n.2035-1G>T