Canonical Allele Identifier: CA359221777

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13794052C>G (hg19) ; chr5:g.13793943C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793943C>G , CM000667.2:g.13793943C>G	GRCh38
NC_000005.9:g.13794052C>G , CM000667.1:g.13794052C>G	GRCh37
NC_000005.8:g.13847052C>G	NCBI36
NG_013081.1:g.155538G>C
NG_013081.2:g.155538G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8003G>C MANE Select	ENSP00000265104.4:p.Gly2668Ala
ENST00000681290.1:c.7958G>C	ENSP00000505288.1:p.Gly2653Ala
ENST00000265104.4:c.8003G>C	ENSP00000265104.4:p.Gly2668Ala
NM_001369.2:c.8003G>C	NP_001360.1:p.Gly2668Ala
XM_005248262.2:c.7958G>C	XP_005248319.1:p.Gly2653Ala
XM_011513990.1:c.8003G>C	XP_011512292.1:p.Gly2668Ala
XR_925598.1:n.8210G>C
XM_005248262.3:c.8111G>C	XP_005248319.2:p.Gly2704Ala
XM_017009177.1:c.8111G>C	XP_016864666.1:p.Gly2704Ala
XM_017009178.1:c.7016G>C	XP_016864667.1:p.Gly2339Ala
XM_017009179.2:c.7016G>C	XP_016864668.1:p.Gly2339Ala
XM_017009180.1:c.8111G>C	XP_016864669.1:p.Gly2704Ala
XM_017009181.1:c.8111G>C	XP_016864670.1:p.Gly2704Ala
XM_017009182.1:c.8111G>C	XP_016864671.1:p.Gly2704Ala
XM_017009183.1:c.8111G>C	XP_016864672.1:p.Gly2704Ala
XM_017009184.1:c.8111G>C	XP_016864673.1:p.Gly2704Ala
XM_017009185.1:c.3200G>C	XP_016864674.1:p.Gly1067Ala
XM_017009186.1:c.2753G>C	XP_016864675.1:p.Gly918Ala
XM_017009188.1:c.2090G>C	XP_016864677.1:p.Gly697Ala
XM_024454388.1:c.7016G>C	XP_024310156.1:p.Gly2339Ala
XM_024454389.1:c.6605G>C	XP_024310157.1:p.Gly2202Ala
XR_001742034.1:n.8128G>C
XR_001742035.1:n.8128G>C
NM_001369.3:c.8003G>C MANE Select	NP_001360.1:p.Gly2668Ala