Canonical Allele Identifier: CA381582262

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047493-A-G
• MyVariant Identifiers: chr11:g.67814960A>G (hg19) ; chr11:g.68047493A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047493A>G , CM000673.2:g.68047493A>G	GRCh38
NC_000011.9:g.67814960A>G , CM000673.1:g.67814960A>G	GRCh37
NC_000011.8:g.67571536A>G	NCBI36
NG_007878.1:g.13478A>G , LRG_115:g.13478A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.755A>G	ENSP00000513629.1:p.His252Arg
ENST00000698255.1:c.1175A>G	ENSP00000513630.1:p.His392Arg
ENST00000698256.1:c.692A>G
ENST00000698257.1:n.644A>G
ENST00000698258.1:n.210A>G
ENST00000698259.1:n.50A>G
ENST00000265686.8:c.1226A>G MANE Select	ENSP00000265686.3:p.His409Arg
ENST00000265686.7:c.1226A>G	ENSP00000265686.3:p.His409Arg
ENST00000525516.1:n.20A>G
ENST00000525724.5:n.538A>G
ENST00000528981.5:c.378A>G
ENST00000529364.1:c.637A>G
ENST00000532635.5:c.578A>G	ENSP00000434407.1:p.His193Arg
ENST00000533005.5:n.262A>G
NM_006019.3:c.1226A>G	NP_006010.2:p.His409Arg
NM_006053.3:c.578A>G	NP_006044.1:p.His193Arg
XM_005273709.2:c.1226A>G	XP_005273766.1:p.His409Arg
XM_011544726.1:c.1226A>G	XP_011543028.1:p.His409Arg
XM_011544727.1:c.1226A>G	XP_011543029.1:p.His409Arg
XM_011544728.1:c.1226A>G	XP_011543030.1:p.His409Arg
XM_011544729.1:c.1242A>G	XP_011543031.1:p.Pro414=
XR_949754.1:n.1230A>G
NM_001351059.1:c.332A>G	NP_001337988.1:p.His111Arg
XM_024448320.1:c.1242A>G	XP_024304088.1:p.Pro414=
XM_024448321.1:c.1242A>G	XP_024304089.1:p.Pro414=
XM_024448322.1:c.1242A>G	XP_024304090.1:p.Pro414=
XM_024448323.1:c.1242A>G	XP_024304091.1:p.Pro414=
XM_024448324.1:c.1242A>G	XP_024304092.1:p.Pro414=
XR_001747721.2:n.1350A>G
XR_001747722.1:n.1363A>G
XR_001747723.2:n.1363A>G
XR_002957115.1:n.1364A>G
NM_006019.4:c.1226A>G MANE Select	NP_006010.2:p.His409Arg
NM_001351059.2:c.332A>G	NP_001337988.1:p.His111Arg
NM_006053.4:c.578A>G	NP_006044.1:p.His193Arg