Canonical Allele Identifier: CA1980429966

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047897C= , CM000673.2:g.68047897C=	GRCh38
NC_000011.9:g.67815364C= , CM000673.1:g.67815364C=	GRCh37
NC_000011.8:g.67571940C=	NCBI36
NG_007878.1:g.13882C= , LRG_115:g.13882C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.104C=
ENST00000698254.1:c.1008C=	ENSP00000513629.1:p.Ala336=
ENST00000698255.1:c.1428C=	ENSP00000513630.1:p.Ala476=
ENST00000698256.1:c.945C=
ENST00000698257.1:n.897C=
ENST00000698258.1:n.614C=
ENST00000698259.1:n.380C=
ENST00000265686.8:c.1479C= MANE Select	ENSP00000265686.3:p.Ala493=
ENST00000265686.7:c.1479C=	ENSP00000265686.3:p.Ala493=
ENST00000525516.1:n.273C=
ENST00000525724.5:n.791C=
ENST00000528981.5:c.631C=
ENST00000532635.5:c.831C=	ENSP00000434407.1:p.Ala277=
ENST00000533005.5:n.592C=
NM_006019.3:c.1479C=	NP_006010.2:p.Ala493=
NM_006053.3:c.831C=	NP_006044.1:p.Ala277=
XM_005273709.2:c.1479C=	XP_005273766.1:p.Ala493=
XM_011544726.1:c.1479C=	XP_011543028.1:p.Ala493=
XM_011544727.1:c.1479C=	XP_011543029.1:p.Ala493=
XM_011544728.1:c.1479C=	XP_011543030.1:p.Ala493=
XR_949754.1:n.1483C=
NM_001351059.1:c.585C=	NP_001337988.1:p.Ala195=
XM_024448320.1:c.1572C=	XP_024304088.1:p.Ala524=
XM_024448321.1:c.1572C=	XP_024304089.1:p.Ala524=
XM_024448322.1:c.1572C=	XP_024304090.1:p.Ala524=
XM_024448323.1:c.1572C=	XP_024304091.1:p.Ala524=
XM_024448324.1:c.1572C=	XP_024304092.1:p.Ala524=
XR_001747721.2:n.1603C=
XR_001747722.1:n.1616C=
XR_001747723.2:n.1616C=
XR_002957115.1:n.1694C=
NM_006019.4:c.1479C= MANE Select	NP_006010.2:p.Ala493=
NM_001351059.2:c.585C=	NP_001337988.1:p.Ala195=
NM_006053.4:c.831C=	NP_006044.1:p.Ala277=