Canonical Allele Identifier: CA1980432187

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048929G= , CM000673.2:g.68048929G=	GRCh38
NC_000011.9:g.67816396G= , CM000673.1:g.67816396G=	GRCh37
NC_000011.8:g.67572972G=	NCBI36
NG_007878.1:g.14914G= , LRG_115:g.14914G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.230G=
ENST00000698254.1:c.1134G=	ENSP00000513629.1:p.Met378=
ENST00000698255.1:c.1554G=	ENSP00000513630.1:p.Met518=
ENST00000698256.1:c.1071G=
ENST00000698257.1:n.1023G=
ENST00000698258.1:n.740G=
ENST00000698259.1:n.506G=
ENST00000265686.8:c.1605G= MANE Select	ENSP00000265686.3:p.Met535=
ENST00000265686.7:c.1605G=	ENSP00000265686.3:p.Met535=
ENST00000525724.5:n.917G=
ENST00000532635.5:c.957G=	ENSP00000434407.1:p.Met319=
ENST00000533005.5:n.718G=
NM_006019.3:c.1605G=	NP_006010.2:p.Met535=
NM_006053.3:c.957G=	NP_006044.1:p.Met319=
XM_005273709.2:c.1605G=	XP_005273766.1:p.Met535=
XM_011544726.1:c.1605G=	XP_011543028.1:p.Met535=
XM_011544727.1:c.1605G=	XP_011543029.1:p.Met535=
XM_011544728.1:c.1605G=	XP_011543030.1:p.Met535=
XR_949754.1:n.1609G=
NM_001351059.1:c.711G=	NP_001337988.1:p.Met237=
XM_024448320.1:c.1698G=	XP_024304088.1:p.Met566=
XM_024448321.1:c.1698G=	XP_024304089.1:p.Met566=
XM_024448322.1:c.1698G=	XP_024304090.1:p.Met566=
XM_024448323.1:c.1698G=	XP_024304091.1:p.Met566=
XM_024448324.1:c.1698G=	XP_024304092.1:p.Met566=
XR_001747721.2:n.1729G=
XR_001747722.1:n.1742G=
XR_001747723.2:n.1742G=
XR_002957115.1:n.1820G=
NM_006019.4:c.1605G= MANE Select	NP_006010.2:p.Met535=
NM_001351059.2:c.711G=	NP_001337988.1:p.Met237=
NM_006053.4:c.957G=	NP_006044.1:p.Met319=