Canonical Allele Identifier: CA381580766

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044293G>A , CM000673.2:g.68044293G>A	GRCh38
NC_000011.9:g.67811760G>A , CM000673.1:g.67811760G>A	GRCh37
NC_000011.8:g.67568336G>A	NCBI36
NG_007878.1:g.10278G>A , LRG_115:g.10278G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.969G>A MANE Select	NP_006010.2:p.Trp323Ter
ENST00000265686.8:c.969G>A MANE Select	ENSP00000265686.3:p.Trp323Ter
NM_001351059.1:c.75G>A	NP_001337988.1:p.Trp25Ter
NM_001351059.2:c.75G>A	NP_001337988.1:p.Trp25Ter
NM_006019.3:c.969G>A	NP_006010.2:p.Trp323Ter
NM_006053.3:c.321G>A	NP_006044.1:p.Trp107Ter
NM_006053.4:c.321G>A	NP_006044.1:p.Trp107Ter
ENST00000265686.7:c.969G>A	ENSP00000265686.3:p.Trp323Ter
ENST00000525724.5:n.281G>A
ENST00000528981.5:c.59G>A
ENST00000529364.1:c.469G>A
ENST00000532635.5:c.321G>A	ENSP00000434407.1:p.Trp107Ter
ENST00000533005.5:n.5G>A
ENST00000698254.1:c.498G>A	ENSP00000513629.1:p.Trp166Ter
ENST00000698255.1:c.918G>A	ENSP00000513630.1:p.Trp306Ter
ENST00000698256.1:c.435G>A
ENST00000698257.1:n.387G>A
XM_005273709.2:c.969G>A	XP_005273766.1:p.Trp323Ter
XM_011544726.1:c.969G>A	XP_011543028.1:p.Trp323Ter
XM_011544727.1:c.969G>A	XP_011543029.1:p.Trp323Ter
XM_011544728.1:c.969G>A	XP_011543030.1:p.Trp323Ter
XM_011544729.1:c.985G>A	XP_011543031.1:p.Val329Met
XM_024448320.1:c.985G>A	XP_024304088.1:p.Val329Met
XM_024448321.1:c.985G>A	XP_024304089.1:p.Val329Met
XM_024448322.1:c.985G>A	XP_024304090.1:p.Val329Met
XM_024448323.1:c.985G>A	XP_024304091.1:p.Val329Met
XM_024448324.1:c.985G>A	XP_024304092.1:p.Val329Met
XR_001747721.2:n.1093G>A
XR_001747722.1:n.1106G>A
XR_001747723.2:n.1106G>A
XR_002957115.1:n.1107G>A
XR_949754.1:n.973G>A