Canonical Allele Identifier: CA359221782

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13794053C>G (hg19) ; chr5:g.13793944C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793944C>G , CM000667.2:g.13793944C>G	GRCh38
NC_000005.9:g.13794053C>G , CM000667.1:g.13794053C>G	GRCh37
NC_000005.8:g.13847053C>G	NCBI36
NG_013081.1:g.155537G>C
NG_013081.2:g.155537G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8002G>C MANE Select	ENSP00000265104.4:p.Gly2668Arg
ENST00000681290.1:c.7957G>C	ENSP00000505288.1:p.Gly2653Arg
ENST00000265104.4:c.8002G>C	ENSP00000265104.4:p.Gly2668Arg
NM_001369.2:c.8002G>C	NP_001360.1:p.Gly2668Arg
XM_005248262.2:c.7957G>C	XP_005248319.1:p.Gly2653Arg
XM_011513990.1:c.8002G>C	XP_011512292.1:p.Gly2668Arg
XR_925598.1:n.8209G>C
XM_005248262.3:c.8110G>C	XP_005248319.2:p.Gly2704Arg
XM_017009177.1:c.8110G>C	XP_016864666.1:p.Gly2704Arg
XM_017009178.1:c.7015G>C	XP_016864667.1:p.Gly2339Arg
XM_017009179.2:c.7015G>C	XP_016864668.1:p.Gly2339Arg
XM_017009180.1:c.8110G>C	XP_016864669.1:p.Gly2704Arg
XM_017009181.1:c.8110G>C	XP_016864670.1:p.Gly2704Arg
XM_017009182.1:c.8110G>C	XP_016864671.1:p.Gly2704Arg
XM_017009183.1:c.8110G>C	XP_016864672.1:p.Gly2704Arg
XM_017009184.1:c.8110G>C	XP_016864673.1:p.Gly2704Arg
XM_017009185.1:c.3199G>C	XP_016864674.1:p.Gly1067Arg
XM_017009186.1:c.2752G>C	XP_016864675.1:p.Gly918Arg
XM_017009188.1:c.2089G>C	XP_016864677.1:p.Gly697Arg
XM_024454388.1:c.7015G>C	XP_024310156.1:p.Gly2339Arg
XM_024454389.1:c.6604G>C	XP_024310157.1:p.Gly2202Arg
XR_001742034.1:n.8127G>C
XR_001742035.1:n.8127G>C
NM_001369.3:c.8002G>C MANE Select	NP_001360.1:p.Gly2668Arg