Canonical Allele Identifier: CA359204647
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13770858T>C , CM000667.2:g.13770858T>C GRCh38
NC_000005.9:g.13770967T>C , CM000667.1:g.13770967T>C GRCh37
NC_000005.8:g.13823967T>C NCBI36
NG_013081.1:g.178623A>G
NG_013081.2:g.178623A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265104.5:c.9496A>G MANE Select ENSP00000265104.4:p.Arg3166Gly
ENST00000681290.1:c.9451A>G ENSP00000505288.1:p.Arg3151Gly
ENST00000265104.4:c.9496A>G ENSP00000265104.4:p.Arg3166Gly
ENST00000504001.3:n.208A>G
NM_001369.2:c.9496A>G NP_001360.1:p.Arg3166Gly
XM_005248262.2:c.9451A>G XP_005248319.1:p.Arg3151Gly
XM_005248262.3:c.9604A>G XP_005248319.2:p.Arg3202Gly
XM_017009177.1:c.9604A>G XP_016864666.1:p.Arg3202Gly
XM_017009178.1:c.8509A>G XP_016864667.1:p.Arg2837Gly
XM_017009179.2:c.8509A>G XP_016864668.1:p.Arg2837Gly
XM_017009180.1:c.9604A>G XP_016864669.1:p.Arg3202Gly
XM_017009181.1:c.9604A>G XP_016864670.1:p.Arg3202Gly
XM_017009182.1:c.9604A>G XP_016864671.1:p.Arg3202Gly
XM_017009183.1:c.9604A>G XP_016864672.1:p.Arg3202Gly
XM_017009185.1:c.4693A>G XP_016864674.1:p.Arg1565Gly
XM_017009186.1:c.4246A>G XP_016864675.1:p.Arg1416Gly
XM_017009188.1:c.3583A>G XP_016864677.1:p.Arg1195Gly
XM_024454388.1:c.8509A>G XP_024310156.1:p.Arg2837Gly
XM_024454389.1:c.8098A>G XP_024310157.1:p.Arg2700Gly
NM_001369.3:c.9496A>G MANE Select NP_001360.1:p.Arg3166Gly