Canonical Allele Identifier: CA1980430221

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047969_68047970delinsTC , CM000673.2:g.68047969_68047970delinsTC	GRCh38
NC_000011.9:g.67815436_67815437delinsTC , CM000673.1:g.67815436_67815437delinsTC	GRCh37
NC_000011.8:g.67572012_67572013delinsTC	NCBI36
NG_007878.1:g.13954_13955delinsTC , LRG_115:g.13954_13955delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.176_177delinsTC
ENST00000698254.1:c.1080_1081delinsTC	ENSP00000513629.1:p.Asp360=
ENST00000698255.1:c.1500_1501delinsTC	ENSP00000513630.1:p.Asp500=
ENST00000698256.1:c.1017_1018delinsTC
ENST00000698257.1:n.969_970delinsTC
ENST00000698258.1:n.686_687delinsTC
ENST00000698259.1:n.452_453delinsTC
ENST00000265686.8:c.1551_1552delinsTC MANE Select	ENSP00000265686.3:p.Asp517=
ENST00000265686.7:c.1551_1552delinsTC	ENSP00000265686.3:p.Asp517=
ENST00000525516.1:n.345_346delinsTC
ENST00000525724.5:n.863_864delinsTC
ENST00000528981.5:c.703_704delinsTC
ENST00000532635.5:c.903_904delinsTC	ENSP00000434407.1:p.Asp301=
ENST00000533005.5:n.664_665delinsTC
NM_006019.3:c.1551_1552delinsTC	NP_006010.2:p.Asp517=
NM_006053.3:c.903_904delinsTC	NP_006044.1:p.Asp301=
XM_005273709.2:c.1551_1552delinsTC	XP_005273766.1:p.Asp517=
XM_011544726.1:c.1551_1552delinsTC	XP_011543028.1:p.Asp517=
XM_011544727.1:c.1551_1552delinsTC	XP_011543029.1:p.Asp517=
XM_011544728.1:c.1551_1552delinsTC	XP_011543030.1:p.Asp517=
XR_949754.1:n.1555_1556delinsTC
NM_001351059.1:c.657_658delinsTC	NP_001337988.1:p.Asp219=
XM_024448320.1:c.1644_1645delinsTC	XP_024304088.1:p.Asp548=
XM_024448321.1:c.1644_1645delinsTC	XP_024304089.1:p.Asp548=
XM_024448322.1:c.1644_1645delinsTC	XP_024304090.1:p.Asp548=
XM_024448323.1:c.1644_1645delinsTC	XP_024304091.1:p.Asp548=
XM_024448324.1:c.1644_1645delinsTC	XP_024304092.1:p.Asp548=
XR_001747721.2:n.1675_1676delinsTC
XR_001747722.1:n.1688_1689delinsTC
XR_001747723.2:n.1688_1689delinsTC
XR_002957115.1:n.1766_1767delinsTC
NM_006019.4:c.1551_1552delinsTC MANE Select	NP_006010.2:p.Asp517=
NM_001351059.2:c.657_658delinsTC	NP_001337988.1:p.Asp219=
NM_006053.4:c.903_904delinsTC	NP_006044.1:p.Asp301=