Canonical Allele Identifier: CA381584525

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815383C>A (hg19) ; chr11:g.68047916C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047916C>A , CM000673.2:g.68047916C>A	GRCh38
NC_000011.9:g.67815383C>A , CM000673.1:g.67815383C>A	GRCh37
NC_000011.8:g.67571959C>A	NCBI36
NG_007878.1:g.13901C>A , LRG_115:g.13901C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.123C>A
ENST00000698254.1:c.1027C>A	ENSP00000513629.1:p.Leu343Met
ENST00000698255.1:c.1447C>A	ENSP00000513630.1:p.Leu483Met
ENST00000698256.1:c.964C>A
ENST00000698257.1:n.916C>A
ENST00000698258.1:n.633C>A
ENST00000698259.1:n.399C>A
ENST00000265686.8:c.1498C>A MANE Select	ENSP00000265686.3:p.Leu500Met
ENST00000265686.7:c.1498C>A	ENSP00000265686.3:p.Leu500Met
ENST00000525516.1:n.292C>A
ENST00000525724.5:n.810C>A
ENST00000528981.5:c.650C>A
ENST00000532635.5:c.850C>A	ENSP00000434407.1:p.Leu284Met
ENST00000533005.5:n.611C>A
NM_006019.3:c.1498C>A	NP_006010.2:p.Leu500Met
NM_006053.3:c.850C>A	NP_006044.1:p.Leu284Met
XM_005273709.2:c.1498C>A	XP_005273766.1:p.Leu500Met
XM_011544726.1:c.1498C>A	XP_011543028.1:p.Leu500Met
XM_011544727.1:c.1498C>A	XP_011543029.1:p.Leu500Met
XM_011544728.1:c.1498C>A	XP_011543030.1:p.Leu500Met
XR_949754.1:n.1502C>A
NM_001351059.1:c.604C>A	NP_001337988.1:p.Leu202Met
XM_024448320.1:c.1591C>A	XP_024304088.1:p.Leu531Met
XM_024448321.1:c.1591C>A	XP_024304089.1:p.Leu531Met
XM_024448322.1:c.1591C>A	XP_024304090.1:p.Leu531Met
XM_024448323.1:c.1591C>A	XP_024304091.1:p.Leu531Met
XM_024448324.1:c.1591C>A	XP_024304092.1:p.Leu531Met
XR_001747721.2:n.1622C>A
XR_001747722.1:n.1635C>A
XR_001747723.2:n.1635C>A
XR_002957115.1:n.1713C>A
NM_006019.4:c.1498C>A MANE Select	NP_006010.2:p.Leu500Met
NM_001351059.2:c.604C>A	NP_001337988.1:p.Leu202Met
NM_006053.4:c.850C>A	NP_006044.1:p.Leu284Met