Canonical Allele Identifier: CA443535916
Gene: DNAH5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.13753561T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13753452T>C , CM000667.2:g.13753452T>C GRCh38
NC_000005.9:g.13753561T>C , CM000667.1:g.13753561T>C GRCh37
NC_000005.8:g.13806561T>C NCBI36
NG_013081.1:g.196029A>G
NG_013081.2:g.196029A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.10653A>G MANE Select ENSP00000265104.4:p.Lys3551=
ENST00000681290.1:c.10608A>G ENSP00000505288.1:p.Lys3536=
ENST00000265104.4:c.10653A>G ENSP00000265104.4:p.Lys3551=
NM_001369.2:c.10653A>G NP_001360.1:p.Lys3551=
XM_005248262.2:c.10608A>G XP_005248319.1:p.Lys3536=
XM_005248262.3:c.10761A>G XP_005248319.2:p.Lys3587=
XM_017009177.1:c.10761A>G XP_016864666.1:p.Lys3587=
XM_017009178.1:c.9666A>G XP_016864667.1:p.Lys3222=
XM_017009179.2:c.9666A>G XP_016864668.1:p.Lys3222=
XM_017009180.1:c.10761A>G XP_016864669.1:p.Lys3587=
XM_017009181.1:c.10761A>G XP_016864670.1:p.Lys3587=
XM_017009182.1:c.10761A>G XP_016864671.1:p.Lys3587=
XM_017009185.1:c.5850A>G XP_016864674.1:p.Lys1950=
XM_017009186.1:c.5403A>G XP_016864675.1:p.Lys1801=
XM_017009188.1:c.4740A>G XP_016864677.1:p.Lys1580=
XM_024454388.1:c.9666A>G XP_024310156.1:p.Lys3222=
XM_024454389.1:c.9255A>G XP_024310157.1:p.Lys3085=
NM_001369.3:c.10653A>G MANE Select NP_001360.1:p.Lys3551=