Canonical Allele Identifier: CA1980430046

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047919G= , CM000673.2:g.68047919G=	GRCh38
NC_000011.9:g.67815386G= , CM000673.1:g.67815386G=	GRCh37
NC_000011.8:g.67571962G=	NCBI36
NG_007878.1:g.13904G= , LRG_115:g.13904G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.126G=
ENST00000698254.1:c.1030G=	ENSP00000513629.1:p.Asp344=
ENST00000698255.1:c.1450G=	ENSP00000513630.1:p.Asp484=
ENST00000698256.1:c.967G=
ENST00000698257.1:n.919G=
ENST00000698258.1:n.636G=
ENST00000698259.1:n.402G=
ENST00000265686.8:c.1501G= MANE Select	ENSP00000265686.3:p.Asp501=
ENST00000265686.7:c.1501G=	ENSP00000265686.3:p.Asp501=
ENST00000525516.1:n.295G=
ENST00000525724.5:n.813G=
ENST00000528981.5:c.653G=
ENST00000532635.5:c.853G=	ENSP00000434407.1:p.Asp285=
ENST00000533005.5:n.614G=
NM_006019.3:c.1501G=	NP_006010.2:p.Asp501=
NM_006053.3:c.853G=	NP_006044.1:p.Asp285=
XM_005273709.2:c.1501G=	XP_005273766.1:p.Asp501=
XM_011544726.1:c.1501G=	XP_011543028.1:p.Asp501=
XM_011544727.1:c.1501G=	XP_011543029.1:p.Asp501=
XM_011544728.1:c.1501G=	XP_011543030.1:p.Asp501=
XR_949754.1:n.1505G=
NM_001351059.1:c.607G=	NP_001337988.1:p.Asp203=
XM_024448320.1:c.1594G=	XP_024304088.1:p.Asp532=
XM_024448321.1:c.1594G=	XP_024304089.1:p.Asp532=
XM_024448322.1:c.1594G=	XP_024304090.1:p.Asp532=
XM_024448323.1:c.1594G=	XP_024304091.1:p.Asp532=
XM_024448324.1:c.1594G=	XP_024304092.1:p.Asp532=
XR_001747721.2:n.1625G=
XR_001747722.1:n.1638G=
XR_001747723.2:n.1638G=
XR_002957115.1:n.1716G=
NM_006019.4:c.1501G= MANE Select	NP_006010.2:p.Asp501=
NM_001351059.2:c.607G=	NP_001337988.1:p.Asp203=
NM_006053.4:c.853G=	NP_006044.1:p.Asp285=