Canonical Allele Identifier: CA1528407030

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717398T= , CM000667.2:g.13717398T=	GRCh38
NC_000005.9:g.13717507T= , CM000667.1:g.13717507T=	GRCh37
NC_000005.8:g.13770507T=	NCBI36
NG_013081.1:g.232083A=
NG_013081.2:g.232083A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.12622A= MANE Select	ENSP00000265104.4:p.Ile4208=
ENST00000681290.1:c.12577A=	ENSP00000505288.1:p.Ile4193=
ENST00000265104.4:c.12622A=	ENSP00000265104.4:p.Ile4208=
NM_001369.2:c.12622A=	NP_001360.1:p.Ile4208=
XM_005248262.2:c.12577A=	XP_005248319.1:p.Ile4193=
XM_005248262.3:c.12730A=	XP_005248319.2:p.Ile4244=
XM_017009177.1:c.12730A=	XP_016864666.1:p.Ile4244=
XM_017009178.1:c.11635A=	XP_016864667.1:p.Ile3879=
XM_017009179.2:c.11635A=	XP_016864668.1:p.Ile3879=
XM_017009180.1:c.12730A=	XP_016864669.1:p.Ile4244=
XM_017009185.1:c.7819A=	XP_016864674.1:p.Ile2607=
XM_017009186.1:c.7372A=	XP_016864675.1:p.Ile2458=
XM_017009188.1:c.6709A=	XP_016864677.1:p.Ile2237=
XM_024454388.1:c.11635A=	XP_024310156.1:p.Ile3879=
XM_024454389.1:c.11224A=	XP_024310157.1:p.Ile3742=
NM_001369.3:c.12622A= MANE Select	NP_001360.1:p.Ile4208=