Canonical Allele Identifier: CA381584409

Gene: TCIRG1

Linked Data

• dbSNP Id: rs2134456014
• gnomAD v4: 11-68047883-G-A
• MyVariant Identifiers: chr11:g.67815350G>A (hg19) ; chr11:g.68047883G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047883G>A , CM000673.2:g.68047883G>A	GRCh38
NC_000011.9:g.67815350G>A , CM000673.1:g.67815350G>A	GRCh37
NC_000011.8:g.67571926G>A	NCBI36
NG_007878.1:g.13868G>A , LRG_115:g.13868G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.90G>A
ENST00000698254.1:c.994G>A	ENSP00000513629.1:p.Asp332Asn
ENST00000698255.1:c.1414G>A	ENSP00000513630.1:p.Asp472Asn
ENST00000698256.1:c.931G>A
ENST00000698257.1:n.883G>A
ENST00000698258.1:n.600G>A
ENST00000698259.1:n.366G>A
ENST00000265686.8:c.1465G>A MANE Select	ENSP00000265686.3:p.Asp489Asn
ENST00000265686.7:c.1465G>A	ENSP00000265686.3:p.Asp489Asn
ENST00000525516.1:n.259G>A
ENST00000525724.5:n.777G>A
ENST00000528981.5:c.617G>A
ENST00000532635.5:c.817G>A	ENSP00000434407.1:p.Asp273Asn
ENST00000533005.5:n.578G>A
NM_006019.3:c.1465G>A	NP_006010.2:p.Asp489Asn
NM_006053.3:c.817G>A	NP_006044.1:p.Asp273Asn
XM_005273709.2:c.1465G>A	XP_005273766.1:p.Asp489Asn
XM_011544726.1:c.1465G>A	XP_011543028.1:p.Asp489Asn
XM_011544727.1:c.1465G>A	XP_011543029.1:p.Asp489Asn
XM_011544728.1:c.1465G>A	XP_011543030.1:p.Asp489Asn
XM_011544729.1:c.1481G>A	XP_011543031.1:p.Ter494=
XR_949754.1:n.1469G>A
NM_001351059.1:c.571G>A	NP_001337988.1:p.Asp191Asn
XM_024448320.1:c.1558G>A	XP_024304088.1:p.Asp520Asn
XM_024448321.1:c.1558G>A	XP_024304089.1:p.Asp520Asn
XM_024448322.1:c.1558G>A	XP_024304090.1:p.Asp520Asn
XM_024448323.1:c.1558G>A	XP_024304091.1:p.Asp520Asn
XM_024448324.1:c.1558G>A	XP_024304092.1:p.Asp520Asn
XR_001747721.2:n.1589G>A
XR_001747722.1:n.1602G>A
XR_001747723.2:n.1602G>A
XR_002957115.1:n.1680G>A
NM_006019.4:c.1465G>A MANE Select	NP_006010.2:p.Asp489Asn
NM_001351059.2:c.571G>A	NP_001337988.1:p.Asp191Asn
NM_006053.4:c.817G>A	NP_006044.1:p.Asp273Asn