Canonical Allele Identifier: CA475513901

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047685-G-A
• MyVariant Identifiers: chr11:g.67815152G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047685G>A , CM000673.2:g.68047685G>A	GRCh38
NC_000011.9:g.67815152G>A , CM000673.1:g.67815152G>A	GRCh37
NC_000011.8:g.67571728G>A	NCBI36
NG_007878.1:g.13670G>A , LRG_115:g.13670G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.873G>A	ENSP00000513629.1:p.Leu291=
ENST00000698255.1:c.1293G>A	ENSP00000513630.1:p.Leu431=
ENST00000698256.1:c.810G>A
ENST00000698257.1:n.762G>A
ENST00000698258.1:n.402G>A
ENST00000698259.1:n.168G>A
ENST00000265686.8:c.1344G>A MANE Select	ENSP00000265686.3:p.Leu448=
ENST00000265686.7:c.1344G>A	ENSP00000265686.3:p.Leu448=
ENST00000525516.1:n.138G>A
ENST00000525724.5:n.656G>A
ENST00000528981.5:c.496G>A
ENST00000529364.1:c.755G>A
ENST00000532635.5:c.696G>A	ENSP00000434407.1:p.Leu232=
ENST00000533005.5:n.380G>A
NM_006019.3:c.1344G>A	NP_006010.2:p.Leu448=
NM_006053.3:c.696G>A	NP_006044.1:p.Leu232=
XM_005273709.2:c.1344G>A	XP_005273766.1:p.Leu448=
XM_011544726.1:c.1344G>A	XP_011543028.1:p.Leu448=
XM_011544727.1:c.1344G>A	XP_011543029.1:p.Leu448=
XM_011544728.1:c.1344G>A	XP_011543030.1:p.Leu448=
XM_011544729.1:c.1360G>A	XP_011543031.1:p.Ala454Thr
XR_949754.1:n.1348G>A
NM_001351059.1:c.450G>A	NP_001337988.1:p.Leu150=
XM_024448320.1:c.1360G>A	XP_024304088.1:p.Ala454Thr
XM_024448321.1:c.1360G>A	XP_024304089.1:p.Ala454Thr
XM_024448322.1:c.1360G>A	XP_024304090.1:p.Ala454Thr
XM_024448323.1:c.1360G>A	XP_024304091.1:p.Ala454Thr
XM_024448324.1:c.1360G>A	XP_024304092.1:p.Ala454Thr
XR_001747721.2:n.1468G>A
XR_001747722.1:n.1481G>A
XR_001747723.2:n.1481G>A
XR_002957115.1:n.1482G>A
NM_006019.4:c.1344G>A MANE Select	NP_006010.2:p.Leu448=
NM_001351059.2:c.450G>A	NP_001337988.1:p.Leu150=
NM_006053.4:c.696G>A	NP_006044.1:p.Leu232=