Canonical Allele Identifier: CA381582242

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047487-T-C
• MyVariant Identifiers: chr11:g.67814954T>C (hg19) ; chr11:g.68047487T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047487T>C , CM000673.2:g.68047487T>C	GRCh38
NC_000011.9:g.67814954T>C , CM000673.1:g.67814954T>C	GRCh37
NC_000011.8:g.67571530T>C	NCBI36
NG_007878.1:g.13472T>C , LRG_115:g.13472T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.749T>C	ENSP00000513629.1:p.Val250Ala
ENST00000698255.1:c.1169T>C	ENSP00000513630.1:p.Val390Ala
ENST00000698256.1:c.686T>C
ENST00000698257.1:n.638T>C
ENST00000698258.1:n.204T>C
ENST00000698259.1:n.44T>C
ENST00000265686.8:c.1220T>C MANE Select	ENSP00000265686.3:p.Val407Ala
ENST00000265686.7:c.1220T>C	ENSP00000265686.3:p.Val407Ala
ENST00000525516.1:n.14T>C
ENST00000525724.5:n.532T>C
ENST00000528981.5:c.372T>C
ENST00000529364.1:c.631T>C
ENST00000532635.5:c.572T>C	ENSP00000434407.1:p.Val191Ala
ENST00000533005.5:n.256T>C
NM_006019.3:c.1220T>C	NP_006010.2:p.Val407Ala
NM_006053.3:c.572T>C	NP_006044.1:p.Val191Ala
XM_005273709.2:c.1220T>C	XP_005273766.1:p.Val407Ala
XM_011544726.1:c.1220T>C	XP_011543028.1:p.Val407Ala
XM_011544727.1:c.1220T>C	XP_011543029.1:p.Val407Ala
XM_011544728.1:c.1220T>C	XP_011543030.1:p.Val407Ala
XM_011544729.1:c.1236T>C	XP_011543031.1:p.Cys412=
XR_949754.1:n.1224T>C
NM_001351059.1:c.326T>C	NP_001337988.1:p.Val109Ala
XM_024448320.1:c.1236T>C	XP_024304088.1:p.Cys412=
XM_024448321.1:c.1236T>C	XP_024304089.1:p.Cys412=
XM_024448322.1:c.1236T>C	XP_024304090.1:p.Cys412=
XM_024448323.1:c.1236T>C	XP_024304091.1:p.Cys412=
XM_024448324.1:c.1236T>C	XP_024304092.1:p.Cys412=
XR_001747721.2:n.1344T>C
XR_001747722.1:n.1357T>C
XR_001747723.2:n.1357T>C
XR_002957115.1:n.1358T>C
NM_006019.4:c.1220T>C MANE Select	NP_006010.2:p.Val407Ala
NM_001351059.2:c.326T>C	NP_001337988.1:p.Val109Ala
NM_006053.4:c.572T>C	NP_006044.1:p.Val191Ala