Canonical Allele Identifier: CA2370487986

Gene: DOK5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54650785_54650793delinsACTTCTCTG , CM000682.2:g.54650785_54650793delinsACTTCTCTG	GRCh38
NC_000020.10:g.53267324_53267332delinsACTTCTCTG , CM000682.1:g.53267324_53267332delinsACTTCTCTG	GRCh37
NC_000020.9:g.52700731_52700739delinsACTTCTCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262593.10:c.*306_*314delinsACTTCTCTG MANE Select	ENSP00000262593.5:n.*306_*314delinsACTTCTCTG
ENST00000262593.9:c.*306_*314delinsACTTCTCTG	ENSP00000262593.5:n.*306_*314delinsACTTCTCTG
ENST00000395939.5:c.*306_*314delinsACTTCTCTG	ENSP00000379270.1:n.*306_*314delinsACTTCTCTG
NM_018431.4:c.*306_*314delinsACTTCTCTG	NP_060901.2:n.*306_*314delinsACTTCTCTG
NM_177959.2:c.*306_*314delinsACTTCTCTG	NP_808874.1:n.*306_*314delinsACTTCTCTG
XM_011528903.1:c.*306_*314delinsACTTCTCTG	XP_011527205.1:n.*306_*314delinsACTTCTCTG
XM_011528904.1:c.*306_*314delinsACTTCTCTG	XP_011527206.1:n.*306_*314delinsACTTCTCTG
XM_024451946.1:c.*306_*314delinsACTTCTCTG	XP_024307714.1:n.*306_*314delinsACTTCTCTG
NM_018431.5:c.*306_*314delinsACTTCTCTG MANE Select	NP_060901.2:n.*306_*314delinsACTTCTCTG
NM_177959.3:c.*306_*314delinsACTTCTCTG	NP_808874.1:n.*306_*314delinsACTTCTCTG