Canonical Allele Identifier: CA381583799

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1245222600
• gnomAD v3: 11-68047702-C-T
• gnomAD v4: 11-68047702-C-T
• MyVariant Identifiers: chr11:g.67815169C>T (hg19) ; chr11:g.68047702C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047702C>T , CM000673.2:g.68047702C>T	GRCh38
NC_000011.9:g.67815169C>T , CM000673.1:g.67815169C>T	GRCh37
NC_000011.8:g.67571745C>T	NCBI36
NG_007878.1:g.13687C>T , LRG_115:g.13687C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.890C>T	ENSP00000513629.1:p.Ser297Phe
ENST00000698255.1:c.1310C>T	ENSP00000513630.1:p.Ser437Phe
ENST00000698256.1:c.827C>T
ENST00000698257.1:n.779C>T
ENST00000698258.1:n.419C>T
ENST00000698259.1:n.185C>T
ENST00000265686.8:c.1361C>T MANE Select	ENSP00000265686.3:p.Ser454Phe
ENST00000265686.7:c.1361C>T	ENSP00000265686.3:p.Ser454Phe
ENST00000525516.1:n.155C>T
ENST00000525724.5:n.673C>T
ENST00000528981.5:c.513C>T
ENST00000529364.1:c.772C>T
ENST00000532635.5:c.713C>T	ENSP00000434407.1:p.Ser238Phe
ENST00000533005.5:n.397C>T
NM_006019.3:c.1361C>T	NP_006010.2:p.Ser454Phe
NM_006053.3:c.713C>T	NP_006044.1:p.Ser238Phe
XM_005273709.2:c.1361C>T	XP_005273766.1:p.Ser454Phe
XM_011544726.1:c.1361C>T	XP_011543028.1:p.Ser454Phe
XM_011544727.1:c.1361C>T	XP_011543029.1:p.Ser454Phe
XM_011544728.1:c.1361C>T	XP_011543030.1:p.Ser454Phe
XM_011544729.1:c.1377C>T	XP_011543031.1:p.Leu459=
XR_949754.1:n.1365C>T
NM_001351059.1:c.467C>T	NP_001337988.1:p.Ser156Phe
XM_024448320.1:c.1377C>T	XP_024304088.1:p.Leu459=
XM_024448321.1:c.1377C>T	XP_024304089.1:p.Leu459=
XM_024448322.1:c.1377C>T	XP_024304090.1:p.Leu459=
XM_024448323.1:c.1377C>T	XP_024304091.1:p.Leu459=
XM_024448324.1:c.1377C>T	XP_024304092.1:p.Leu459=
XR_001747721.2:n.1485C>T
XR_001747722.1:n.1498C>T
XR_001747723.2:n.1498C>T
XR_002957115.1:n.1499C>T
NM_006019.4:c.1361C>T MANE Select	NP_006010.2:p.Ser454Phe
NM_001351059.2:c.467C>T	NP_001337988.1:p.Ser156Phe
NM_006053.4:c.713C>T	NP_006044.1:p.Ser238Phe