Canonical Allele Identifier: CA475447334

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044164G>A , CM000673.2:g.68044164G>A	GRCh38
NC_000011.9:g.67811631G>A , CM000673.1:g.67811631G>A	GRCh37
NC_000011.8:g.67568207G>A	NCBI36
NG_007878.1:g.10149G>A , LRG_115:g.10149G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.840G>A MANE Select	NP_006010.2:p.Gln280=
ENST00000265686.8:c.840G>A MANE Select	ENSP00000265686.3:p.Gln280=
NM_001351059.1:c.-55G>A	NP_001337988.1:n.-55G>A
NM_001351059.2:c.-55G>A	NP_001337988.1:n.-55G>A
NM_006019.3:c.840G>A	NP_006010.2:p.Gln280=
NM_006053.3:c.192G>A	NP_006044.1:p.Gln64=
NM_006053.4:c.192G>A	NP_006044.1:p.Gln64=
ENST00000265686.7:c.840G>A	ENSP00000265686.3:p.Gln280=
ENST00000524598.5:c.798G>A	ENSP00000432846.1:p.Gln266=
ENST00000525724.5:n.152G>A
ENST00000527530.1:n.458G>A
ENST00000529364.1:c.340G>A
ENST00000532635.5:c.192G>A	ENSP00000434407.1:p.Gln64=
ENST00000534673.5:c.*188G>A	ENSP00000431174.1:n.*188G>A
ENST00000698254.1:c.404-35G>A	ENSP00000513629.1:n.404-35G>A
ENST00000698255.1:c.789G>A	ENSP00000513630.1:p.Gln263=
ENST00000698256.1:c.306G>A
ENST00000698257.1:n.258G>A
XM_005273709.2:c.840G>A	XP_005273766.1:p.Gln280=
XM_011544726.1:c.840G>A	XP_011543028.1:p.Gln280=
XM_011544727.1:c.840G>A	XP_011543029.1:p.Gln280=
XM_011544728.1:c.840G>A	XP_011543030.1:p.Gln280=
XM_011544729.1:c.856G>A	XP_011543031.1:p.Gly286Ser
XM_024448320.1:c.856G>A	XP_024304088.1:p.Gly286Ser
XM_024448321.1:c.856G>A	XP_024304089.1:p.Gly286Ser
XM_024448322.1:c.856G>A	XP_024304090.1:p.Gly286Ser
XM_024448323.1:c.856G>A	XP_024304091.1:p.Gly286Ser
XM_024448324.1:c.856G>A	XP_024304092.1:p.Gly286Ser
XR_001747721.2:n.964G>A
XR_001747722.1:n.977G>A
XR_001747723.2:n.977G>A
XR_002957115.1:n.978G>A
XR_949754.1:n.844G>A