Canonical Allele Identifier: CA1882768236

Gene: DBH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133636738_133636741delinsCAAA , CM000671.2:g.133636738_133636741delinsCAAA	GRCh38
NC_000009.11:g.136501860_136501863delinsCAAA , CM000671.1:g.136501860_136501863delinsCAAA	GRCh37
NC_000009.10:g.135491681_135491684delinsCAAA	NCBI36
NG_008645.1:g.5376_5379delinsCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263611.3:c.333+28_333+31delinsCAAA	ENSP00000263611.3:n.333+28_333+31delinsCAAA
ENST00000393056.8:c.339+28_339+31delinsCAAA MANE Select	ENSP00000376776.2:n.339+28_339+31delinsCAAA
ENST00000263611.2:c.297+28_297+31delinsCAAA	ENSP00000263611.2:n.297+28_297+31delinsCAAA
ENST00000393056.6:c.339+28_339+31delinsCAAA	ENSP00000376776.2:n.339+28_339+31delinsCAAA
NM_000787.3:c.339+28_339+31delinsCAAA	NP_000778.3:n.339+28_339+31delinsCAAA
NM_000787.4:c.339+28_339+31delinsCAAA MANE Select	NP_000778.3:n.339+28_339+31delinsCAAA