Canonical Allele Identifier: CA1948003180

Gene: TH

Linked Data

• dbSNP Id: rs1846047199

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2165026del , CM000673.2:g.2165026del	GRCh38
NC_000011.9:g.2186256del , CM000673.1:g.2186256del	GRCh37
NC_000011.8:g.2142832del	NCBI36
NG_007114.1:g.1173del
NG_008128.1:g.11784del
NG_050578.1:g.1188del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.1334+210del MANE Select	ENSP00000325951.4:n.1334+210del
ENST00000333684.9:c.1052+210del	ENSP00000328814.6:n.1052+210del
ENST00000352909.7:c.1334+210del	ENSP00000325951.3:n.1334+210del
ENST00000381175.5:c.1415+210del	ENSP00000370567.1:n.1415+210del
ENST00000381178.5:c.1427+210del	ENSP00000370571.1:n.1427+210del
NM_000360.3:c.1334+210del	NP_000351.2:n.1334+210del
NM_199292.2:c.1427+210del	NP_954986.2:n.1427+210del
NM_199293.2:c.1415+210del	NP_954987.2:n.1415+210del
XM_011520335.1:c.1346+210del	XP_011518637.1:n.1346+210del
XM_011520335.2:c.1346+210del	XP_011518637.1:n.1346+210del
NM_000360.4:c.1334+210del MANE Select	NP_000351.2:n.1334+210del
NM_199292.3:c.1427+210del	NP_954986.2:n.1427+210del
NM_199293.3:c.1415+210del	NP_954987.2:n.1415+210del