Canonical Allele Identifier: CA381574984
Community Standard Title: NM_006019.4(TCIRG1):c.196+1G>T
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68041832G>T , CM000673.2:g.68041832G>T GRCh38
NC_000011.9:g.67809299G>T , CM000673.1:g.67809299G>T GRCh37
NC_000011.8:g.67565875G>T NCBI36
NG_007878.1:g.7817G>T , LRG_115:g.7817G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006019.4:c.196+1G>T MANE Select NP_006010.2:n.196+1G>T
ENST00000265686.8:c.196+1G>T MANE Select ENSP00000265686.3:n.196+1G>T
NM_001351059.1:c.-1054+1G>T NP_001337988.1:n.-1054+1G>T
NM_001351059.2:c.-1054+1G>T NP_001337988.1:n.-1054+1G>T
NM_006019.3:c.196+1G>T NP_006010.2:n.196+1G>T
ENST00000265686.7:c.196+1G>T ENSP00000265686.3:n.196+1G>T
ENST00000524598.5:c.154+1G>T ENSP00000432846.1:n.154+1G>T
ENST00000529657.1:c.196+1G>T ENSP00000435023.1:n.196+1G>T
ENST00000533947.1:n.163+1G>T
ENST00000534673.5:c.196+1G>T ENSP00000431174.1:n.196+1G>T
ENST00000698254.1:c.196+1G>T ENSP00000513629.1:n.196+1G>T
ENST00000698255.1:c.196+1G>T ENSP00000513630.1:n.196+1G>T
XM_005273709.2:c.196+1G>T XP_005273766.1:n.196+1G>T
XM_011544726.1:c.196+1G>T XP_011543028.1:n.196+1G>T
XM_011544727.1:c.196+1G>T XP_011543029.1:n.196+1G>T
XM_011544728.1:c.196+1G>T XP_011543030.1:n.196+1G>T
XM_011544729.1:c.196+1G>T XP_011543031.1:n.196+1G>T
XM_024448320.1:c.196+1G>T XP_024304088.1:n.196+1G>T
XM_024448321.1:c.196+1G>T XP_024304089.1:n.196+1G>T
XM_024448322.1:c.196+1G>T XP_024304090.1:n.196+1G>T
XM_024448323.1:c.196+1G>T XP_024304091.1:n.196+1G>T
XM_024448324.1:c.196+1G>T XP_024304092.1:n.196+1G>T
XR_001747721.2:n.320+1G>T
XR_001747722.1:n.317+1G>T
XR_001747723.2:n.317+1G>T
XR_002957115.1:n.318+1G>T
XR_949754.1:n.200+1G>T