Canonical Allele Identifier: CA443248844

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13692240T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692131T>C , CM000667.2:g.13692131T>C	GRCh38
NC_000005.9:g.13692240T>C , CM000667.1:g.13692240T>C	GRCh37
NC_000005.8:g.13745240T>C	NCBI36
NG_013081.1:g.257350A>G
NG_013081.2:g.257350A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1061A>G
ENST00000265104.5:c.13728A>G MANE Select	ENSP00000265104.4:p.Leu4576=
ENST00000681290.1:c.13683A>G	ENSP00000505288.1:p.Leu4561=
ENST00000265104.4:c.13728A>G	ENSP00000265104.4:p.Leu4576=
NM_001369.2:c.13728A>G	NP_001360.1:p.Leu4576=
XM_005248262.2:c.13683A>G	XP_005248319.1:p.Leu4561=
XM_005248262.3:c.13836A>G	XP_005248319.2:p.Leu4612=
XM_017009177.1:c.13416A>G	XP_016864666.1:p.Leu4472=
XM_017009178.1:c.12741A>G	XP_016864667.1:p.Leu4247=
XM_017009179.2:c.12741A>G	XP_016864668.1:p.Leu4247=
XM_017009185.1:c.8925A>G	XP_016864674.1:p.Leu2975=
XM_017009186.1:c.8478A>G	XP_016864675.1:p.Leu2826=
XM_017009188.1:c.7815A>G	XP_016864677.1:p.Leu2605=
XM_024454388.1:c.12741A>G	XP_024310156.1:p.Leu4247=
XM_024454389.1:c.12330A>G	XP_024310157.1:p.Leu4110=
NM_001369.3:c.13728A>G MANE Select	NP_001360.1:p.Leu4576=