Canonical Allele Identifier: CA475513874

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815349T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047882T>C , CM000673.2:g.68047882T>C	GRCh38
NC_000011.9:g.67815349T>C , CM000673.1:g.67815349T>C	GRCh37
NC_000011.8:g.67571925T>C	NCBI36
NG_007878.1:g.13867T>C , LRG_115:g.13867T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.89T>C
ENST00000698254.1:c.993T>C	ENSP00000513629.1:p.Ser331=
ENST00000698255.1:c.1413T>C	ENSP00000513630.1:p.Ser471=
ENST00000698256.1:c.930T>C
ENST00000698257.1:n.882T>C
ENST00000698258.1:n.599T>C
ENST00000698259.1:n.365T>C
ENST00000265686.8:c.1464T>C MANE Select	ENSP00000265686.3:p.Ser488=
ENST00000265686.7:c.1464T>C	ENSP00000265686.3:p.Ser488=
ENST00000525516.1:n.258T>C
ENST00000525724.5:n.776T>C
ENST00000528981.5:c.616T>C
ENST00000532635.5:c.816T>C	ENSP00000434407.1:p.Ser272=
ENST00000533005.5:n.577T>C
NM_006019.3:c.1464T>C	NP_006010.2:p.Ser488=
NM_006053.3:c.816T>C	NP_006044.1:p.Ser272=
XM_005273709.2:c.1464T>C	XP_005273766.1:p.Ser488=
XM_011544726.1:c.1464T>C	XP_011543028.1:p.Ser488=
XM_011544727.1:c.1464T>C	XP_011543029.1:p.Ser488=
XM_011544728.1:c.1464T>C	XP_011543030.1:p.Ser488=
XM_011544729.1:c.1480T>C	XP_011543031.1:p.Ter494Arg
XR_949754.1:n.1468T>C
NM_001351059.1:c.570T>C	NP_001337988.1:p.Ser190=
XM_024448320.1:c.1557T>C	XP_024304088.1:p.Ser519=
XM_024448321.1:c.1557T>C	XP_024304089.1:p.Ser519=
XM_024448322.1:c.1557T>C	XP_024304090.1:p.Ser519=
XM_024448323.1:c.1557T>C	XP_024304091.1:p.Ser519=
XM_024448324.1:c.1557T>C	XP_024304092.1:p.Ser519=
XR_001747721.2:n.1588T>C
XR_001747722.1:n.1601T>C
XR_001747723.2:n.1601T>C
XR_002957115.1:n.1679T>C
NM_006019.4:c.1464T>C MANE Select	NP_006010.2:p.Ser488=
NM_001351059.2:c.570T>C	NP_001337988.1:p.Ser190=
NM_006053.4:c.816T>C	NP_006044.1:p.Ser272=