Canonical Allele Identifier: CA1980431900

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048837G= , CM000673.2:g.68048837G=	GRCh38
NC_000011.9:g.67816304G= , CM000673.1:g.67816304G=	GRCh37
NC_000011.8:g.67572880G=	NCBI36
NG_007878.1:g.14822G= , LRG_115:g.14822G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.180-42G=
ENST00000698254.1:c.1084-42G=	ENSP00000513629.1:n.1084-42G=
ENST00000698255.1:c.1504-42G=	ENSP00000513630.1:n.1504-42G=
ENST00000698256.1:c.1021-42G=
ENST00000698257.1:n.973-42G=
ENST00000698258.1:n.690-42G=
ENST00000698259.1:n.456-42G=
ENST00000265686.8:c.1555-42G= MANE Select	ENSP00000265686.3:n.1555-42G=
ENST00000265686.7:c.1555-42G=	ENSP00000265686.3:n.1555-42G=
ENST00000525724.5:n.867-42G=
ENST00000528981.5:c.707-42G=
ENST00000532635.5:c.907-42G=	ENSP00000434407.1:n.907-42G=
ENST00000533005.5:n.668-42G=
NM_006019.3:c.1555-42G=	NP_006010.2:n.1555-42G=
NM_006053.3:c.907-42G=	NP_006044.1:n.907-42G=
XM_005273709.2:c.1555-42G=	XP_005273766.1:n.1555-42G=
XM_011544726.1:c.1555-42G=	XP_011543028.1:n.1555-42G=
XM_011544727.1:c.1555-42G=	XP_011543029.1:n.1555-42G=
XM_011544728.1:c.1555-42G=	XP_011543030.1:n.1555-42G=
XR_949754.1:n.1559-42G=
NM_001351059.1:c.661-42G=	NP_001337988.1:n.661-42G=
XM_024448320.1:c.1648-42G=	XP_024304088.1:n.1648-42G=
XM_024448321.1:c.1648-42G=	XP_024304089.1:n.1648-42G=
XM_024448322.1:c.1648-42G=	XP_024304090.1:n.1648-42G=
XM_024448323.1:c.1648-42G=	XP_024304091.1:n.1648-42G=
XM_024448324.1:c.1648-42G=	XP_024304092.1:n.1648-42G=
XR_001747721.2:n.1679-42G=
XR_001747722.1:n.1692-42G=
XR_001747723.2:n.1692-42G=
XR_002957115.1:n.1770-42G=
NM_006019.4:c.1555-42G= MANE Select	NP_006010.2:n.1555-42G=
NM_001351059.2:c.661-42G=	NP_001337988.1:n.661-42G=
NM_006053.4:c.907-42G=	NP_006044.1:n.907-42G=