Canonical Allele Identifier: CA804439020

Gene: DNAH5

Linked Data

• dbSNP Id: rs1454743130
• MyVariant Identifiers: chr5:g.13752401_13752402insG (hg19) ; chr5:g.13752292_13752293insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752294dup , CM000667.2:g.13752294dup	GRCh38
NC_000005.9:g.13752403dup , CM000667.1:g.13752403dup	GRCh37
NC_000005.8:g.13805403dup	NCBI36
NG_013081.1:g.197188dup
NG_013081.2:g.197188dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10873-4dup MANE Select	ENSP00000265104.4:n.10873-4dup
ENST00000681290.1:c.10828-4dup	ENSP00000505288.1:n.10828-4dup
ENST00000265104.4:c.10873-4dup	ENSP00000265104.4:n.10873-4dup
NM_001369.2:c.10873-4dup	NP_001360.1:n.10873-4dup
XM_005248262.2:c.10828-4dup	XP_005248319.1:n.10828-4dup
XM_005248262.3:c.10981-4dup	XP_005248319.2:n.10981-4dup
XM_017009177.1:c.10981-4dup	XP_016864666.1:n.10981-4dup
XM_017009178.1:c.9886-4dup	XP_016864667.1:n.9886-4dup
XM_017009179.2:c.9886-4dup	XP_016864668.1:n.9886-4dup
XM_017009180.1:c.10981-4dup	XP_016864669.1:n.10981-4dup
XM_017009181.1:c.10981-4dup	XP_016864670.1:n.10981-4dup
XM_017009182.1:c.10981-4dup	XP_016864671.1:n.10981-4dup
XM_017009185.1:c.6070-4dup	XP_016864674.1:n.6070-4dup
XM_017009186.1:c.5623-4dup	XP_016864675.1:n.5623-4dup
XM_017009188.1:c.4960-4dup	XP_016864677.1:n.4960-4dup
XM_024454388.1:c.9886-4dup	XP_024310156.1:n.9886-4dup
XM_024454389.1:c.9475-4dup	XP_024310157.1:n.9475-4dup
NM_001369.3:c.10873-4dup MANE Select	NP_001360.1:n.10873-4dup