Canonical Allele Identifier: CA381578463
Community Standard Title: NM_006019.4(TCIRG1):c.647G>A (p.Trp216Ter)
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68043587G>A , CM000673.2:g.68043587G>A GRCh38
NC_000011.9:g.67811054G>A , CM000673.1:g.67811054G>A GRCh37
NC_000011.8:g.67567630G>A NCBI36
NG_007878.1:g.9572G>A , LRG_115:g.9572G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006019.4:c.647G>A MANE Select NP_006010.2:p.Trp216Ter
ENST00000265686.8:c.647G>A MANE Select ENSP00000265686.3:p.Trp216Ter
NM_001351059.1:c.-264G>A NP_001337988.1:n.-264G>A
NM_001351059.2:c.-264G>A NP_001337988.1:n.-264G>A
NM_006019.3:c.647G>A NP_006010.2:p.Trp216Ter
NM_006053.3:c.-2G>A NP_006044.1:n.-2G>A
NM_006053.4:c.-2G>A NP_006044.1:n.-2G>A
ENST00000265686.7:c.647G>A ENSP00000265686.3:p.Trp216Ter
ENST00000524598.5:c.605G>A ENSP00000432846.1:p.Trp202Ter
ENST00000527530.1:n.265G>A
ENST00000529364.1:c.147G>A
ENST00000529657.1:c.647G>A ENSP00000435023.1:p.Trp216Ter
ENST00000532635.5:c.-2G>A ENSP00000434407.1:n.-2G>A
ENST00000533947.1:n.953G>A
ENST00000534673.5:c.520G>A ENSP00000431174.1:p.Gly174Arg
ENST00000698254.1:c.404-612G>A ENSP00000513629.1:n.404-612G>A
ENST00000698255.1:c.631-35G>A ENSP00000513630.1:n.631-35G>A
ENST00000698256.1:c.97G>A
ENST00000698257.1:n.65G>A
XM_005273709.2:c.647G>A XP_005273766.1:p.Trp216Ter
XM_011544726.1:c.647G>A XP_011543028.1:p.Trp216Ter
XM_011544727.1:c.647G>A XP_011543029.1:p.Trp216Ter
XM_011544728.1:c.647G>A XP_011543030.1:p.Trp216Ter
XM_011544729.1:c.647G>A XP_011543031.1:p.Trp216Ter
XM_024448320.1:c.647G>A XP_024304088.1:p.Trp216Ter
XM_024448321.1:c.647G>A XP_024304089.1:p.Trp216Ter
XM_024448322.1:c.647G>A XP_024304090.1:p.Trp216Ter
XM_024448323.1:c.647G>A XP_024304091.1:p.Trp216Ter
XM_024448324.1:c.647G>A XP_024304092.1:p.Trp216Ter
XR_001747721.2:n.771G>A
XR_001747722.1:n.768G>A
XR_001747723.2:n.768G>A
XR_002957115.1:n.769G>A
XR_949754.1:n.651G>A