Canonical Allele Identifier: CA2579501753

Gene: DBH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133636738_133636739insCTG , CM000671.2:g.133636738_133636739insCTG	GRCh38
NC_000009.11:g.136501860_136501861insCTG , CM000671.1:g.136501860_136501861insCTG	GRCh37
NC_000009.10:g.135491681_135491682insCTG	NCBI36
NG_008645.1:g.5376_5377insCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000263611.3:c.333+28_333+29insCTG	ENSP00000263611.3:n.333+28_333+29insCTG
ENST00000393056.8:c.339+28_339+29insCTG MANE Select	ENSP00000376776.2:n.339+28_339+29insCTG
ENST00000263611.2:c.297+28_297+29insCTG	ENSP00000263611.2:n.297+28_297+29insCTG
ENST00000393056.6:c.339+28_339+29insCTG	ENSP00000376776.2:n.339+28_339+29insCTG
NM_000787.3:c.339+28_339+29insCTG	NP_000778.3:n.339+28_339+29insCTG
NM_000787.4:c.339+28_339+29insCTG MANE Select	NP_000778.3:n.339+28_339+29insCTG