Canonical Allele Identifier: CA381584961

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816367C>G (hg19) ; chr11:g.68048900C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048900C>G , CM000673.2:g.68048900C>G	GRCh38
NC_000011.9:g.67816367C>G , CM000673.1:g.67816367C>G	GRCh37
NC_000011.8:g.67572943C>G	NCBI36
NG_007878.1:g.14885C>G , LRG_115:g.14885C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.201C>G
ENST00000698254.1:c.1105C>G	ENSP00000513629.1:p.His369Asp
ENST00000698255.1:c.1525C>G	ENSP00000513630.1:p.His509Asp
ENST00000698256.1:c.1042C>G
ENST00000698257.1:n.994C>G
ENST00000698258.1:n.711C>G
ENST00000698259.1:n.477C>G
ENST00000265686.8:c.1576C>G MANE Select	ENSP00000265686.3:p.His526Asp
ENST00000265686.7:c.1576C>G	ENSP00000265686.3:p.His526Asp
ENST00000525724.5:n.888C>G
ENST00000528981.5:c.728C>G
ENST00000532635.5:c.928C>G	ENSP00000434407.1:p.His310Asp
ENST00000533005.5:n.689C>G
NM_006019.3:c.1576C>G	NP_006010.2:p.His526Asp
NM_006053.3:c.928C>G	NP_006044.1:p.His310Asp
XM_005273709.2:c.1576C>G	XP_005273766.1:p.His526Asp
XM_011544726.1:c.1576C>G	XP_011543028.1:p.His526Asp
XM_011544727.1:c.1576C>G	XP_011543029.1:p.His526Asp
XM_011544728.1:c.1576C>G	XP_011543030.1:p.His526Asp
XR_949754.1:n.1580C>G
NM_001351059.1:c.682C>G	NP_001337988.1:p.His228Asp
XM_024448320.1:c.1669C>G	XP_024304088.1:p.His557Asp
XM_024448321.1:c.1669C>G	XP_024304089.1:p.His557Asp
XM_024448322.1:c.1669C>G	XP_024304090.1:p.His557Asp
XM_024448323.1:c.1669C>G	XP_024304091.1:p.His557Asp
XM_024448324.1:c.1669C>G	XP_024304092.1:p.His557Asp
XR_001747721.2:n.1700C>G
XR_001747722.1:n.1713C>G
XR_001747723.2:n.1713C>G
XR_002957115.1:n.1791C>G
NM_006019.4:c.1576C>G MANE Select	NP_006010.2:p.His526Asp
NM_001351059.2:c.682C>G	NP_001337988.1:p.His228Asp
NM_006053.4:c.928C>G	NP_006044.1:p.His310Asp