Canonical Allele Identifier: CA381580958

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044345G>T , CM000673.2:g.68044345G>T	GRCh38
NC_000011.9:g.67811812G>T , CM000673.1:g.67811812G>T	GRCh37
NC_000011.8:g.67568388G>T	NCBI36
NG_007878.1:g.10330G>T , LRG_115:g.10330G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1020+1G>T MANE Select	NP_006010.2:n.1020+1G>T
ENST00000265686.8:c.1020+1G>T MANE Select	ENSP00000265686.3:n.1020+1G>T
NM_001351059.1:c.126+1G>T	NP_001337988.1:n.126+1G>T
NM_001351059.2:c.126+1G>T	NP_001337988.1:n.126+1G>T
NM_006019.3:c.1020+1G>T	NP_006010.2:n.1020+1G>T
NM_006053.3:c.372+1G>T	NP_006044.1:n.372+1G>T
NM_006053.4:c.372+1G>T	NP_006044.1:n.372+1G>T
ENST00000265686.7:c.1020+1G>T	ENSP00000265686.3:n.1020+1G>T
ENST00000525724.5:n.332+1G>T
ENST00000528981.5:c.110+1G>T
ENST00000529364.1:c.520+1G>T
ENST00000532635.5:c.372+1G>T	ENSP00000434407.1:n.372+1G>T
ENST00000533005.5:n.56+1G>T
ENST00000698254.1:c.549+1G>T	ENSP00000513629.1:n.549+1G>T
ENST00000698255.1:c.969+1G>T	ENSP00000513630.1:n.969+1G>T
ENST00000698256.1:c.486+1G>T
ENST00000698257.1:n.438+1G>T
XM_005273709.2:c.1020+1G>T	XP_005273766.1:n.1020+1G>T
XM_011544726.1:c.1020+1G>T	XP_011543028.1:n.1020+1G>T
XM_011544727.1:c.1020+1G>T	XP_011543029.1:n.1020+1G>T
XM_011544728.1:c.1020+1G>T	XP_011543030.1:n.1020+1G>T
XM_011544729.1:c.1036+1G>T	XP_011543031.1:n.1036+1G>T
XM_024448320.1:c.1036+1G>T	XP_024304088.1:n.1036+1G>T
XM_024448321.1:c.1036+1G>T	XP_024304089.1:n.1036+1G>T
XM_024448322.1:c.1036+1G>T	XP_024304090.1:n.1036+1G>T
XM_024448323.1:c.1036+1G>T	XP_024304091.1:n.1036+1G>T
XM_024448324.1:c.1036+1G>T	XP_024304092.1:n.1036+1G>T
XR_001747721.2:n.1144+1G>T
XR_001747722.1:n.1157+1G>T
XR_001747723.2:n.1157+1G>T
XR_002957115.1:n.1158+1G>T
XR_949754.1:n.1024+1G>T