Canonical Allele Identifier: CA17875811

Gene: TARDBP

Linked Data

• dbSNP Id: rs963088629
• gnomAD v3: 1-11021979-G-C
• gnomAD v4: 1-11021979-G-C
• MyVariant Identifiers: chr1:g.11082036G>C (hg19) ; chr1:g.11021979G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11021979G>C , CM000663.2:g.11021979G>C	GRCh38
NC_000001.10:g.11082036G>C , CM000663.1:g.11082036G>C	GRCh37
NC_000001.9:g.11004623G>C	NCBI36
NG_008734.1:g.14358G>C , LRG_659:g.14358G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240185.8:c.715-145G>C MANE Select	ENSP00000240185.4:n.715-145G>C
ENST00000639083.1:c.715-145G>C	ENSP00000491203.1:n.715-145G>C
ENST00000639599.1:c.715-145G>C	ENSP00000492196.1:n.715-145G>C
ENST00000649624.1:c.715-145G>C	ENSP00000497327.1:n.715-145G>C
ENST00000240185.7:c.715-145G>C	ENSP00000240185.3:n.715-145G>C
ENST00000315091.7:c.715-145G>C	ENSP00000313129.3:n.715-145G>C
ENST00000439080.6:c.*296-145G>C	ENSP00000404666.3:n.*296-145G>C
ENST00000472476.5:c.*604-145G>C	ENSP00000465080.1:n.*604-145G>C
ENST00000473869.5:c.715-145G>C	ENSP00000432132.1:n.715-145G>C
ENST00000477447.6:c.14-145G>C
ENST00000610369.4:c.193-145G>C	ENSP00000482559.1:n.193-145G>C
ENST00000611136.4:c.95-145G>C
ENST00000611963.4:c.355-145G>C	ENSP00000481330.1:n.355-145G>C
ENST00000614494.1:c.168-145G>C
ENST00000614757.4:c.715-145G>C	ENSP00000481867.1:n.715-145G>C
ENST00000616545.4:c.715-145G>C	ENSP00000484722.1:n.715-145G>C
ENST00000617172.4:c.456-145G>C
ENST00000619555.4:c.266-145G>C
ENST00000620632.4:c.266-145G>C
ENST00000621715.4:c.544-145G>C	ENSP00000480690.1:n.544-145G>C
ENST00000621790.4:c.715-145G>C	ENSP00000482191.1:n.715-145G>C
ENST00000622057.4:c.462-145G>C
ENST00000629725.2:c.715-145G>C	ENSP00000486989.1:n.715-145G>C
NM_007375.3:c.715-145G>C , LRG_659t1:c.715-145G>C	NP_031401.1:n.715-145G>C
XR_946596.1:n.837-145G>C
XR_946597.1:n.837-145G>C
XM_017000863.2:c.715-145G>C	XP_016856352.1:n.715-145G>C
XM_017000864.2:c.715-145G>C	XP_016856353.1:n.715-145G>C
XM_017000865.2:c.715-145G>C	XP_016856354.1:n.715-145G>C
XM_017000866.2:c.715-145G>C	XP_016856355.1:n.715-145G>C
XM_017000867.2:c.715-145G>C	XP_016856356.1:n.715-145G>C
XM_017000868.2:c.715-145G>C	XP_016856357.1:n.715-145G>C
NM_007375.4:c.715-145G>C MANE Select	NP_031401.1:n.715-145G>C