Canonical Allele Identifier: CA1980432174

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048927A= , CM000673.2:g.68048927A=	GRCh38
NC_000011.9:g.67816394A= , CM000673.1:g.67816394A=	GRCh37
NC_000011.8:g.67572970A=	NCBI36
NG_007878.1:g.14912A= , LRG_115:g.14912A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.228A=
ENST00000698254.1:c.1132A=	ENSP00000513629.1:p.Met378=
ENST00000698255.1:c.1552A=	ENSP00000513630.1:p.Met518=
ENST00000698256.1:c.1069A=
ENST00000698257.1:n.1021A=
ENST00000698258.1:n.738A=
ENST00000698259.1:n.504A=
ENST00000265686.8:c.1603A= MANE Select	ENSP00000265686.3:p.Met535=
ENST00000265686.7:c.1603A=	ENSP00000265686.3:p.Met535=
ENST00000525724.5:n.915A=
ENST00000528981.5:c.755A=
ENST00000532635.5:c.955A=	ENSP00000434407.1:p.Met319=
ENST00000533005.5:n.716A=
NM_006019.3:c.1603A=	NP_006010.2:p.Met535=
NM_006053.3:c.955A=	NP_006044.1:p.Met319=
XM_005273709.2:c.1603A=	XP_005273766.1:p.Met535=
XM_011544726.1:c.1603A=	XP_011543028.1:p.Met535=
XM_011544727.1:c.1603A=	XP_011543029.1:p.Met535=
XM_011544728.1:c.1603A=	XP_011543030.1:p.Met535=
XR_949754.1:n.1607A=
NM_001351059.1:c.709A=	NP_001337988.1:p.Met237=
XM_024448320.1:c.1696A=	XP_024304088.1:p.Met566=
XM_024448321.1:c.1696A=	XP_024304089.1:p.Met566=
XM_024448322.1:c.1696A=	XP_024304090.1:p.Met566=
XM_024448323.1:c.1696A=	XP_024304091.1:p.Met566=
XM_024448324.1:c.1696A=	XP_024304092.1:p.Met566=
XR_001747721.2:n.1727A=
XR_001747722.1:n.1740A=
XR_001747723.2:n.1740A=
XR_002957115.1:n.1818A=
NM_006019.4:c.1603A= MANE Select	NP_006010.2:p.Met535=
NM_001351059.2:c.709A=	NP_001337988.1:p.Met237=
NM_006053.4:c.955A=	NP_006044.1:p.Met319=