Canonical Allele Identifier: CA2740093072

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 2963544
• ClinVar RCV Id: RCV003823198

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047864T>C , CM000673.2:g.68047864T>C	GRCh38
NC_000011.9:g.67815331T>C , CM000673.1:g.67815331T>C	GRCh37
NC_000011.8:g.67571907T>C	NCBI36
NG_007878.1:g.13849T>C , LRG_115:g.13849T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.89-18T>C
ENST00000698254.1:c.993-18T>C	ENSP00000513629.1:n.993-18T>C
ENST00000698255.1:c.1413-18T>C	ENSP00000513630.1:n.1413-18T>C
ENST00000698256.1:c.930-18T>C
ENST00000698257.1:n.882-18T>C
ENST00000698258.1:n.581T>C
ENST00000698259.1:n.347T>C
ENST00000265686.8:c.1464-18T>C MANE Select	ENSP00000265686.3:n.1464-18T>C
ENST00000265686.7:c.1464-18T>C	ENSP00000265686.3:n.1464-18T>C
ENST00000525516.1:n.258-18T>C
ENST00000525724.5:n.776-18T>C
ENST00000528981.5:c.616-18T>C
ENST00000532635.5:c.816-18T>C	ENSP00000434407.1:n.816-18T>C
ENST00000533005.5:n.559T>C
NM_006019.3:c.1464-18T>C	NP_006010.2:n.1464-18T>C
NM_006053.3:c.816-18T>C	NP_006044.1:n.816-18T>C
XM_005273709.2:c.1464-18T>C	XP_005273766.1:n.1464-18T>C
XM_011544726.1:c.1464-18T>C	XP_011543028.1:n.1464-18T>C
XM_011544727.1:c.1464-18T>C	XP_011543029.1:n.1464-18T>C
XM_011544728.1:c.1464-18T>C	XP_011543030.1:n.1464-18T>C
XM_011544729.1:c.1480-18T>C	XP_011543031.1:n.1480-18T>C
XR_949754.1:n.1468-18T>C
NM_001351059.1:c.570-18T>C	NP_001337988.1:n.570-18T>C
XM_024448320.1:c.1539T>C	XP_024304088.1:p.Pro513=
XM_024448321.1:c.1539T>C	XP_024304089.1:p.Pro513=
XM_024448322.1:c.1539T>C	XP_024304090.1:p.Pro513=
XM_024448323.1:c.1539T>C	XP_024304091.1:p.Pro513=
XM_024448324.1:c.1539T>C	XP_024304092.1:p.Pro513=
XR_001747721.2:n.1588-18T>C
XR_001747722.1:n.1601-18T>C
XR_001747723.2:n.1601-18T>C
XR_002957115.1:n.1661T>C
NM_006019.4:c.1464-18T>C MANE Select	NP_006010.2:n.1464-18T>C
NM_001351059.2:c.570-18T>C	NP_001337988.1:n.570-18T>C
NM_006053.4:c.816-18T>C	NP_006044.1:n.816-18T>C