Canonical Allele Identifier: CA381584452

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047893-T-C
• MyVariant Identifiers: chr11:g.67815360T>C (hg19) ; chr11:g.68047893T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047893T>C , CM000673.2:g.68047893T>C	GRCh38
NC_000011.9:g.67815360T>C , CM000673.1:g.67815360T>C	GRCh37
NC_000011.8:g.67571936T>C	NCBI36
NG_007878.1:g.13878T>C , LRG_115:g.13878T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.100T>C
ENST00000698254.1:c.1004T>C	ENSP00000513629.1:p.Leu335Pro
ENST00000698255.1:c.1424T>C	ENSP00000513630.1:p.Leu475Pro
ENST00000698256.1:c.941T>C
ENST00000698257.1:n.893T>C
ENST00000698258.1:n.610T>C
ENST00000698259.1:n.376T>C
ENST00000265686.8:c.1475T>C MANE Select	ENSP00000265686.3:p.Leu492Pro
ENST00000265686.7:c.1475T>C	ENSP00000265686.3:p.Leu492Pro
ENST00000525516.1:n.269T>C
ENST00000525724.5:n.787T>C
ENST00000528981.5:c.627T>C
ENST00000532635.5:c.827T>C	ENSP00000434407.1:p.Leu276Pro
ENST00000533005.5:n.588T>C
NM_006019.3:c.1475T>C	NP_006010.2:p.Leu492Pro
NM_006053.3:c.827T>C	NP_006044.1:p.Leu276Pro
XM_005273709.2:c.1475T>C	XP_005273766.1:p.Leu492Pro
XM_011544726.1:c.1475T>C	XP_011543028.1:p.Leu492Pro
XM_011544727.1:c.1475T>C	XP_011543029.1:p.Leu492Pro
XM_011544728.1:c.1475T>C	XP_011543030.1:p.Leu492Pro
XM_011544729.1:c.*9T>C	XP_011543031.1:n.*9T>C
XR_949754.1:n.1479T>C
NM_001351059.1:c.581T>C	NP_001337988.1:p.Leu194Pro
XM_024448320.1:c.1568T>C	XP_024304088.1:p.Leu523Pro
XM_024448321.1:c.1568T>C	XP_024304089.1:p.Leu523Pro
XM_024448322.1:c.1568T>C	XP_024304090.1:p.Leu523Pro
XM_024448323.1:c.1568T>C	XP_024304091.1:p.Leu523Pro
XM_024448324.1:c.1568T>C	XP_024304092.1:p.Leu523Pro
XR_001747721.2:n.1599T>C
XR_001747722.1:n.1612T>C
XR_001747723.2:n.1612T>C
XR_002957115.1:n.1690T>C
NM_006019.4:c.1475T>C MANE Select	NP_006010.2:p.Leu492Pro
NM_001351059.2:c.581T>C	NP_001337988.1:p.Leu194Pro
NM_006053.4:c.827T>C	NP_006044.1:p.Leu276Pro