Canonical Allele Identifier: CA381580757

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044292G>A , CM000673.2:g.68044292G>A	GRCh38
NC_000011.9:g.67811759G>A , CM000673.1:g.67811759G>A	GRCh37
NC_000011.8:g.67568335G>A	NCBI36
NG_007878.1:g.10277G>A , LRG_115:g.10277G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.968G>A MANE Select	NP_006010.2:p.Trp323Ter
ENST00000265686.8:c.968G>A MANE Select	ENSP00000265686.3:p.Trp323Ter
NM_001351059.1:c.74G>A	NP_001337988.1:p.Trp25Ter
NM_001351059.2:c.74G>A	NP_001337988.1:p.Trp25Ter
NM_006019.3:c.968G>A	NP_006010.2:p.Trp323Ter
NM_006053.3:c.320G>A	NP_006044.1:p.Trp107Ter
NM_006053.4:c.320G>A	NP_006044.1:p.Trp107Ter
ENST00000265686.7:c.968G>A	ENSP00000265686.3:p.Trp323Ter
ENST00000525724.5:n.280G>A
ENST00000528981.5:c.58G>A
ENST00000529364.1:c.468G>A
ENST00000532635.5:c.320G>A	ENSP00000434407.1:p.Trp107Ter
ENST00000533005.5:n.4G>A
ENST00000698254.1:c.497G>A	ENSP00000513629.1:p.Trp166Ter
ENST00000698255.1:c.917G>A	ENSP00000513630.1:p.Trp306Ter
ENST00000698256.1:c.434G>A
ENST00000698257.1:n.386G>A
XM_005273709.2:c.968G>A	XP_005273766.1:p.Trp323Ter
XM_011544726.1:c.968G>A	XP_011543028.1:p.Trp323Ter
XM_011544727.1:c.968G>A	XP_011543029.1:p.Trp323Ter
XM_011544728.1:c.968G>A	XP_011543030.1:p.Trp323Ter
XM_011544729.1:c.984G>A	XP_011543031.1:p.Leu328=
XM_024448320.1:c.984G>A	XP_024304088.1:p.Leu328=
XM_024448321.1:c.984G>A	XP_024304089.1:p.Leu328=
XM_024448322.1:c.984G>A	XP_024304090.1:p.Leu328=
XM_024448323.1:c.984G>A	XP_024304091.1:p.Leu328=
XM_024448324.1:c.984G>A	XP_024304092.1:p.Leu328=
XR_001747721.2:n.1092G>A
XR_001747722.1:n.1105G>A
XR_001747723.2:n.1105G>A
XR_002957115.1:n.1106G>A
XR_949754.1:n.972G>A