Canonical Allele Identifier: CA649754907

Gene: DNAH5

Linked Data

• COSMIC: COSN21336732

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13691626_13691627insA , CM000667.2:g.13691626_13691627insA	GRCh38
NC_000005.9:g.13691735_13691736insA , CM000667.1:g.13691735_13691736insA	GRCh37
NC_000005.8:g.13744735_13744736insA	NCBI36
NG_013081.1:g.257854_257855insT
NG_013081.2:g.257854_257855insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1565_1566insT
ENST00000265104.5:c.*357_*358insT MANE Select	ENSP00000265104.4:n.*357_*358insT
ENST00000681290.1:c.*357_*358insT	ENSP00000505288.1:n.*357_*358insT
ENST00000265104.4:c.*357_*358insT	ENSP00000265104.4:n.*357_*358insT
NM_001369.2:c.*357_*358insT	NP_001360.1:n.*357_*358insT
XM_005248262.2:c.*357_*358insT	XP_005248319.1:n.*357_*358insT
XM_005248262.3:c.*357_*358insT	XP_005248319.2:n.*357_*358insT
XM_017009177.1:c.*357_*358insT	XP_016864666.1:n.*357_*358insT
XM_017009178.1:c.*357_*358insT	XP_016864667.1:n.*357_*358insT
XM_017009179.2:c.*357_*358insT	XP_016864668.1:n.*357_*358insT
XM_017009185.1:c.*357_*358insT	XP_016864674.1:n.*357_*358insT
XM_017009186.1:c.*357_*358insT	XP_016864675.1:n.*357_*358insT
XM_017009188.1:c.*357_*358insT	XP_016864677.1:n.*357_*358insT
XM_024454388.1:c.*357_*358insT	XP_024310156.1:n.*357_*358insT
XM_024454389.1:c.*357_*358insT	XP_024310157.1:n.*357_*358insT
NM_001369.3:c.*357_*358insT MANE Select	NP_001360.1:n.*357_*358insT