Canonical Allele Identifier: CA381582222

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67814950G>C (hg19) ; chr11:g.68047483G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047483G>C , CM000673.2:g.68047483G>C	GRCh38
NC_000011.9:g.67814950G>C , CM000673.1:g.67814950G>C	GRCh37
NC_000011.8:g.67571526G>C	NCBI36
NG_007878.1:g.13468G>C , LRG_115:g.13468G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.745G>C	ENSP00000513629.1:p.Asp249His
ENST00000698255.1:c.1165G>C	ENSP00000513630.1:p.Asp389His
ENST00000698256.1:c.682G>C
ENST00000698257.1:n.634G>C
ENST00000698258.1:n.200G>C
ENST00000698259.1:n.40G>C
ENST00000265686.8:c.1216G>C MANE Select	ENSP00000265686.3:p.Asp406His
ENST00000265686.7:c.1216G>C	ENSP00000265686.3:p.Asp406His
ENST00000525516.1:n.10G>C
ENST00000525724.5:n.528G>C
ENST00000528981.5:c.368G>C
ENST00000529364.1:c.627G>C
ENST00000532635.5:c.568G>C	ENSP00000434407.1:p.Asp190His
ENST00000533005.5:n.252G>C
NM_006019.3:c.1216G>C	NP_006010.2:p.Asp406His
NM_006053.3:c.568G>C	NP_006044.1:p.Asp190His
XM_005273709.2:c.1216G>C	XP_005273766.1:p.Asp406His
XM_011544726.1:c.1216G>C	XP_011543028.1:p.Asp406His
XM_011544727.1:c.1216G>C	XP_011543029.1:p.Asp406His
XM_011544728.1:c.1216G>C	XP_011543030.1:p.Asp406His
XM_011544729.1:c.1232G>C	XP_011543031.1:p.Gly411Ala
XR_949754.1:n.1220G>C
NM_001351059.1:c.322G>C	NP_001337988.1:p.Asp108His
XM_024448320.1:c.1232G>C	XP_024304088.1:p.Gly411Ala
XM_024448321.1:c.1232G>C	XP_024304089.1:p.Gly411Ala
XM_024448322.1:c.1232G>C	XP_024304090.1:p.Gly411Ala
XM_024448323.1:c.1232G>C	XP_024304091.1:p.Gly411Ala
XM_024448324.1:c.1232G>C	XP_024304092.1:p.Gly411Ala
XR_001747721.2:n.1340G>C
XR_001747722.1:n.1353G>C
XR_001747723.2:n.1353G>C
XR_002957115.1:n.1354G>C
NM_006019.4:c.1216G>C MANE Select	NP_006010.2:p.Asp406His
NM_001351059.2:c.322G>C	NP_001337988.1:p.Asp108His
NM_006053.4:c.568G>C	NP_006044.1:p.Asp190His