Canonical Allele Identifier: CA359223203

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13735333C>G (hg19) ; chr5:g.13735224C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735224C>G , CM000667.2:g.13735224C>G	GRCh38
NC_000005.9:g.13735333C>G , CM000667.1:g.13735333C>G	GRCh37
NC_000005.8:g.13788333C>G	NCBI36
NG_013081.1:g.214257G>C
NG_013081.2:g.214257G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.11668G>C MANE Select	ENSP00000265104.4:p.Glu3890Gln
ENST00000681290.1:c.11623G>C	ENSP00000505288.1:p.Glu3875Gln
ENST00000265104.4:c.11668G>C	ENSP00000265104.4:p.Glu3890Gln
NM_001369.2:c.11668G>C	NP_001360.1:p.Glu3890Gln
XM_005248262.2:c.11623G>C	XP_005248319.1:p.Glu3875Gln
XM_005248262.3:c.11776G>C	XP_005248319.2:p.Glu3926Gln
XM_017009177.1:c.11776G>C	XP_016864666.1:p.Glu3926Gln
XM_017009178.1:c.10681G>C	XP_016864667.1:p.Glu3561Gln
XM_017009179.2:c.10681G>C	XP_016864668.1:p.Glu3561Gln
XM_017009180.1:c.11776G>C	XP_016864669.1:p.Glu3926Gln
XM_017009181.1:c.11776G>C	XP_016864670.1:p.Glu3926Gln
XM_017009185.1:c.6865G>C	XP_016864674.1:p.Glu2289Gln
XM_017009186.1:c.6418G>C	XP_016864675.1:p.Glu2140Gln
XM_017009188.1:c.5755G>C	XP_016864677.1:p.Glu1919Gln
XM_024454388.1:c.10681G>C	XP_024310156.1:p.Glu3561Gln
XM_024454389.1:c.10270G>C	XP_024310157.1:p.Glu3424Gln
NM_001369.3:c.11668G>C MANE Select	NP_001360.1:p.Glu3890Gln