Canonical Allele Identifier: CA224208599

Gene: TCIRG1

Linked Data

• dbSNP Id: rs201443254
• gnomAD v4: 11-68047902-A-C
• MyVariant Identifiers: chr11:g.67815369A>C (hg19) ; chr11:g.68047902A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047902A>C , CM000673.2:g.68047902A>C	GRCh38
NC_000011.9:g.67815369A>C , CM000673.1:g.67815369A>C	GRCh37
NC_000011.8:g.67571945A>C	NCBI36
NG_007878.1:g.13887A>C , LRG_115:g.13887A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.109A>C
ENST00000698254.1:c.1013A>C	ENSP00000513629.1:p.His338Pro
ENST00000698255.1:c.1433A>C	ENSP00000513630.1:p.His478Pro
ENST00000698256.1:c.950A>C
ENST00000698257.1:n.902A>C
ENST00000698258.1:n.619A>C
ENST00000698259.1:n.385A>C
ENST00000265686.8:c.1484A>C MANE Select	ENSP00000265686.3:p.His495Pro
ENST00000265686.7:c.1484A>C	ENSP00000265686.3:p.His495Pro
ENST00000525516.1:n.278A>C
ENST00000525724.5:n.796A>C
ENST00000528981.5:c.636A>C
ENST00000532635.5:c.836A>C	ENSP00000434407.1:p.His279Pro
ENST00000533005.5:n.597A>C
NM_006019.3:c.1484A>C	NP_006010.2:p.His495Pro
NM_006053.3:c.836A>C	NP_006044.1:p.His279Pro
XM_005273709.2:c.1484A>C	XP_005273766.1:p.His495Pro
XM_011544726.1:c.1484A>C	XP_011543028.1:p.His495Pro
XM_011544727.1:c.1484A>C	XP_011543029.1:p.His495Pro
XM_011544728.1:c.1484A>C	XP_011543030.1:p.His495Pro
XR_949754.1:n.1488A>C
NM_001351059.1:c.590A>C	NP_001337988.1:p.His197Pro
XM_024448320.1:c.1577A>C	XP_024304088.1:p.His526Pro
XM_024448321.1:c.1577A>C	XP_024304089.1:p.His526Pro
XM_024448322.1:c.1577A>C	XP_024304090.1:p.His526Pro
XM_024448323.1:c.1577A>C	XP_024304091.1:p.His526Pro
XM_024448324.1:c.1577A>C	XP_024304092.1:p.His526Pro
XR_001747721.2:n.1608A>C
XR_001747722.1:n.1621A>C
XR_001747723.2:n.1621A>C
XR_002957115.1:n.1699A>C
NM_006019.4:c.1484A>C MANE Select	NP_006010.2:p.His495Pro
NM_001351059.2:c.590A>C	NP_001337988.1:p.His197Pro
NM_006053.4:c.836A>C	NP_006044.1:p.His279Pro