Canonical Allele Identifier: CA1528407084

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717520C= , CM000667.2:g.13717520C=	GRCh38
NC_000005.9:g.13717629C= , CM000667.1:g.13717629C=	GRCh37
NC_000005.8:g.13770629C=	NCBI36
NG_013081.1:g.231961G=
NG_013081.2:g.231961G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.12500G= MANE Select	ENSP00000265104.4:p.Gly4167=
ENST00000681290.1:c.12455G=	ENSP00000505288.1:p.Gly4152=
ENST00000265104.4:c.12500G=	ENSP00000265104.4:p.Gly4167=
NM_001369.2:c.12500G=	NP_001360.1:p.Gly4167=
XM_005248262.2:c.12455G=	XP_005248319.1:p.Gly4152=
XM_005248262.3:c.12608G=	XP_005248319.2:p.Gly4203=
XM_017009177.1:c.12608G=	XP_016864666.1:p.Gly4203=
XM_017009178.1:c.11513G=	XP_016864667.1:p.Gly3838=
XM_017009179.2:c.11513G=	XP_016864668.1:p.Gly3838=
XM_017009180.1:c.12608G=	XP_016864669.1:p.Gly4203=
XM_017009185.1:c.7697G=	XP_016864674.1:p.Gly2566=
XM_017009186.1:c.7250G=	XP_016864675.1:p.Gly2417=
XM_017009188.1:c.6587G=	XP_016864677.1:p.Gly2196=
XM_024454388.1:c.11513G=	XP_024310156.1:p.Gly3838=
XM_024454389.1:c.11102G=	XP_024310157.1:p.Gly3701=
NM_001369.3:c.12500G= MANE Select	NP_001360.1:p.Gly4167=