Canonical Allele Identifier: CA381584677

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047968-A-T
• MyVariant Identifiers: chr11:g.67815435A>T (hg19) ; chr11:g.68047968A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047968A>T , CM000673.2:g.68047968A>T	GRCh38
NC_000011.9:g.67815435A>T , CM000673.1:g.67815435A>T	GRCh37
NC_000011.8:g.67572011A>T	NCBI36
NG_007878.1:g.13953A>T , LRG_115:g.13953A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.175A>T
ENST00000698254.1:c.1079A>T	ENSP00000513629.1:p.Asp360Val
ENST00000698255.1:c.1499A>T	ENSP00000513630.1:p.Asp500Val
ENST00000698256.1:c.1016A>T
ENST00000698257.1:n.968A>T
ENST00000698258.1:n.685A>T
ENST00000698259.1:n.451A>T
ENST00000265686.8:c.1550A>T MANE Select	ENSP00000265686.3:p.Asp517Val
ENST00000265686.7:c.1550A>T	ENSP00000265686.3:p.Asp517Val
ENST00000525516.1:n.344A>T
ENST00000525724.5:n.862A>T
ENST00000528981.5:c.702A>T
ENST00000532635.5:c.902A>T	ENSP00000434407.1:p.Asp301Val
ENST00000533005.5:n.663A>T
NM_006019.3:c.1550A>T	NP_006010.2:p.Asp517Val
NM_006053.3:c.902A>T	NP_006044.1:p.Asp301Val
XM_005273709.2:c.1550A>T	XP_005273766.1:p.Asp517Val
XM_011544726.1:c.1550A>T	XP_011543028.1:p.Asp517Val
XM_011544727.1:c.1550A>T	XP_011543029.1:p.Asp517Val
XM_011544728.1:c.1550A>T	XP_011543030.1:p.Asp517Val
XR_949754.1:n.1554A>T
NM_001351059.1:c.656A>T	NP_001337988.1:p.Asp219Val
XM_024448320.1:c.1643A>T	XP_024304088.1:p.Asp548Val
XM_024448321.1:c.1643A>T	XP_024304089.1:p.Asp548Val
XM_024448322.1:c.1643A>T	XP_024304090.1:p.Asp548Val
XM_024448323.1:c.1643A>T	XP_024304091.1:p.Asp548Val
XM_024448324.1:c.1643A>T	XP_024304092.1:p.Asp548Val
XR_001747721.2:n.1674A>T
XR_001747722.1:n.1687A>T
XR_001747723.2:n.1687A>T
XR_002957115.1:n.1765A>T
NM_006019.4:c.1550A>T MANE Select	NP_006010.2:p.Asp517Val
NM_001351059.2:c.656A>T	NP_001337988.1:p.Asp219Val
NM_006053.4:c.902A>T	NP_006044.1:p.Asp301Val