Canonical Allele Identifier: CA475514086

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047763-G-C
• MyVariant Identifiers: chr11:g.67815230G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047763G>C , CM000673.2:g.68047763G>C	GRCh38
NC_000011.9:g.67815230G>C , CM000673.1:g.67815230G>C	GRCh37
NC_000011.8:g.67571806G>C	NCBI36
NG_007878.1:g.13748G>C , LRG_115:g.13748G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.47G>C
ENST00000698254.1:c.951G>C	ENSP00000513629.1:p.Ser317=
ENST00000698255.1:c.1371G>C	ENSP00000513630.1:p.Ser457=
ENST00000698256.1:c.888G>C
ENST00000698257.1:n.840G>C
ENST00000698258.1:n.480G>C
ENST00000698259.1:n.246G>C
ENST00000265686.8:c.1422G>C MANE Select	ENSP00000265686.3:p.Ser474=
ENST00000265686.7:c.1422G>C	ENSP00000265686.3:p.Ser474=
ENST00000525516.1:n.216G>C
ENST00000525724.5:n.734G>C
ENST00000528981.5:c.574G>C
ENST00000529364.1:c.833G>C
ENST00000532635.5:c.774G>C	ENSP00000434407.1:p.Ser258=
ENST00000533005.5:n.458G>C
NM_006019.3:c.1422G>C	NP_006010.2:p.Ser474=
NM_006053.3:c.774G>C	NP_006044.1:p.Ser258=
XM_005273709.2:c.1422G>C	XP_005273766.1:p.Ser474=
XM_011544726.1:c.1422G>C	XP_011543028.1:p.Ser474=
XM_011544727.1:c.1422G>C	XP_011543029.1:p.Ser474=
XM_011544728.1:c.1422G>C	XP_011543030.1:p.Ser474=
XM_011544729.1:c.1438G>C	XP_011543031.1:p.Gly480Arg
XR_949754.1:n.1426G>C
NM_001351059.1:c.528G>C	NP_001337988.1:p.Ser176=
XM_024448320.1:c.1438G>C	XP_024304088.1:p.Gly480Arg
XM_024448321.1:c.1438G>C	XP_024304089.1:p.Gly480Arg
XM_024448322.1:c.1438G>C	XP_024304090.1:p.Gly480Arg
XM_024448323.1:c.1438G>C	XP_024304091.1:p.Gly480Arg
XM_024448324.1:c.1438G>C	XP_024304092.1:p.Gly480Arg
XR_001747721.2:n.1546G>C
XR_001747722.1:n.1559G>C
XR_001747723.2:n.1559G>C
XR_002957115.1:n.1560G>C
NM_006019.4:c.1422G>C MANE Select	NP_006010.2:p.Ser474=
NM_001351059.2:c.528G>C	NP_001337988.1:p.Ser176=
NM_006053.4:c.774G>C	NP_006044.1:p.Ser258=