Canonical Allele Identifier: CA381589142

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68049961G>A , CM000673.2:g.68049961G>A	GRCh38
NC_000011.9:g.67817428G>A , CM000673.1:g.67817428G>A	GRCh37
NC_000011.8:g.67574004G>A	NCBI36
NG_007878.1:g.15946G>A , LRG_115:g.15946G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2014-1G>A MANE Select	NP_006010.2:n.2014-1G>A
ENST00000265686.8:c.2014-1G>A MANE Select	ENSP00000265686.3:n.2014-1G>A
NM_001351059.1:c.1120-1G>A	NP_001337988.1:n.1120-1G>A
NM_001351059.2:c.1120-1G>A	NP_001337988.1:n.1120-1G>A
NM_006019.3:c.2014-1G>A	NP_006010.2:n.2014-1G>A
NM_006053.3:c.1366-1G>A	NP_006044.1:n.1366-1G>A
NM_006053.4:c.1366-1G>A	NP_006044.1:n.1366-1G>A
ENST00000265686.7:c.2014-1G>A	ENSP00000265686.3:n.2014-1G>A
ENST00000524870.1:n.642-1G>A
ENST00000525724.5:n.1326-1G>A
ENST00000530449.2:n.1007-1G>A
ENST00000532635.5:c.1366-1G>A	ENSP00000434407.1:n.1366-1G>A
ENST00000533005.5:n.1127-1G>A
ENST00000698254.1:c.1543-1G>A	ENSP00000513629.1:n.1543-1G>A
ENST00000698255.1:c.1963-1G>A	ENSP00000513630.1:n.1963-1G>A
ENST00000698256.1:c.1480-1G>A
ENST00000698257.1:n.1432-1G>A
ENST00000698258.1:n.1149-1G>A
ENST00000698259.1:n.1283-1G>A
XM_005273709.2:c.2014-1G>A	XP_005273766.1:n.2014-1G>A
XM_011544726.1:c.2014-1G>A	XP_011543028.1:n.2014-1G>A
XM_011544727.1:c.2014-1G>A	XP_011543029.1:n.2014-1G>A
XM_024448320.1:c.2107-1G>A	XP_024304088.1:n.2107-1G>A
XM_024448321.1:c.2107-1G>A	XP_024304089.1:n.2107-1G>A
XM_024448322.1:c.2107-1G>A	XP_024304090.1:n.2107-1G>A
XM_024448323.1:c.2107-1G>A	XP_024304091.1:n.2107-1G>A
XR_001747721.2:n.2183-1G>A
XR_001747722.1:n.2151-1G>A
XR_001747723.2:n.2196-1G>A
XR_002957115.1:n.2372-1G>A
XR_949754.1:n.2161-1G>A