Canonical Allele Identifier: CA359195085
Community Standard Title: NM_001369.3(DNAH5):c.2947A>T (p.Lys983Ter)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13885025T>A , CM000667.2:g.13885025T>A GRCh38
NC_000005.9:g.13885134T>A , CM000667.1:g.13885134T>A GRCh37
NC_000005.8:g.13938134T>A NCBI36
NG_013081.1:g.64456A>T
NG_013081.2:g.64456A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.2947A>T MANE Select NP_001360.1:p.Lys983Ter
ENST00000265104.5:c.2947A>T MANE Select ENSP00000265104.4:p.Lys983Ter
NM_001369.2:c.2947A>T NP_001360.1:p.Lys983Ter
ENST00000265104.4:c.2947A>T ENSP00000265104.4:p.Lys983Ter
ENST00000681290.1:c.2902A>T ENSP00000505288.1:p.Lys968Ter
XM_005248262.2:c.2902A>T XP_005248319.1:p.Lys968Ter
XM_005248262.3:c.3055A>T XP_005248319.2:p.Lys1019Ter
XM_011513990.1:c.2947A>T XP_011512292.1:p.Lys983Ter
XM_017009177.1:c.3055A>T XP_016864666.1:p.Lys1019Ter
XM_017009178.1:c.1960A>T XP_016864667.1:p.Lys654Ter
XM_017009179.2:c.1960A>T XP_016864668.1:p.Lys654Ter
XM_017009180.1:c.3055A>T XP_016864669.1:p.Lys1019Ter
XM_017009181.1:c.3055A>T XP_016864670.1:p.Lys1019Ter
XM_017009182.1:c.3055A>T XP_016864671.1:p.Lys1019Ter
XM_017009183.1:c.3055A>T XP_016864672.1:p.Lys1019Ter
XM_017009184.1:c.3055A>T XP_016864673.1:p.Lys1019Ter
XM_017009187.1:c.3055A>T XP_016864676.1:p.Lys1019Ter
XM_024454388.1:c.1960A>T XP_024310156.1:p.Lys654Ter
XM_024454389.1:c.1549A>T XP_024310157.1:p.Lys517Ter
XR_001742034.1:n.3072A>T
XR_001742035.1:n.3072A>T
XR_925598.1:n.3154A>T