Canonical Allele Identifier: CA381582259

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047492-C-T
• MyVariant Identifiers: chr11:g.67814959C>T (hg19) ; chr11:g.68047492C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047492C>T , CM000673.2:g.68047492C>T	GRCh38
NC_000011.9:g.67814959C>T , CM000673.1:g.67814959C>T	GRCh37
NC_000011.8:g.67571535C>T	NCBI36
NG_007878.1:g.13477C>T , LRG_115:g.13477C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.754C>T	ENSP00000513629.1:p.His252Tyr
ENST00000698255.1:c.1174C>T	ENSP00000513630.1:p.His392Tyr
ENST00000698256.1:c.691C>T
ENST00000698257.1:n.643C>T
ENST00000698258.1:n.209C>T
ENST00000698259.1:n.49C>T
ENST00000265686.8:c.1225C>T MANE Select	ENSP00000265686.3:p.His409Tyr
ENST00000265686.7:c.1225C>T	ENSP00000265686.3:p.His409Tyr
ENST00000525516.1:n.19C>T
ENST00000525724.5:n.537C>T
ENST00000528981.5:c.377C>T
ENST00000529364.1:c.636C>T
ENST00000532635.5:c.577C>T	ENSP00000434407.1:p.His193Tyr
ENST00000533005.5:n.261C>T
NM_006019.3:c.1225C>T	NP_006010.2:p.His409Tyr
NM_006053.3:c.577C>T	NP_006044.1:p.His193Tyr
XM_005273709.2:c.1225C>T	XP_005273766.1:p.His409Tyr
XM_011544726.1:c.1225C>T	XP_011543028.1:p.His409Tyr
XM_011544727.1:c.1225C>T	XP_011543029.1:p.His409Tyr
XM_011544728.1:c.1225C>T	XP_011543030.1:p.His409Tyr
XM_011544729.1:c.1241C>T	XP_011543031.1:p.Pro414Leu
XR_949754.1:n.1229C>T
NM_001351059.1:c.331C>T	NP_001337988.1:p.His111Tyr
XM_024448320.1:c.1241C>T	XP_024304088.1:p.Pro414Leu
XM_024448321.1:c.1241C>T	XP_024304089.1:p.Pro414Leu
XM_024448322.1:c.1241C>T	XP_024304090.1:p.Pro414Leu
XM_024448323.1:c.1241C>T	XP_024304091.1:p.Pro414Leu
XM_024448324.1:c.1241C>T	XP_024304092.1:p.Pro414Leu
XR_001747721.2:n.1349C>T
XR_001747722.1:n.1362C>T
XR_001747723.2:n.1362C>T
XR_002957115.1:n.1363C>T
NM_006019.4:c.1225C>T MANE Select	NP_006010.2:p.His409Tyr
NM_001351059.2:c.331C>T	NP_001337988.1:p.His111Tyr
NM_006053.4:c.577C>T	NP_006044.1:p.His193Tyr