Canonical Allele Identifier: CA3204483
Community Standard Title: NM_001369.3(DNAH5):c.2779T>C (p.Ser927Pro)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13885193A>G , CM000667.2:g.13885193A>G GRCh38
NC_000005.9:g.13885302A>G , CM000667.1:g.13885302A>G GRCh37
NC_000005.8:g.13938302A>G NCBI36
NG_013081.1:g.64288T>C
NG_013081.2:g.64288T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.2779T>C MANE Select NP_001360.1:p.Ser927Pro
ENST00000265104.5:c.2779T>C MANE Select ENSP00000265104.4:p.Ser927Pro
NM_001369.2:c.2779T>C NP_001360.1:p.Ser927Pro
ENST00000265104.4:c.2779T>C ENSP00000265104.4:p.Ser927Pro
ENST00000681290.1:c.2734T>C ENSP00000505288.1:p.Ser912Pro
XM_005248262.2:c.2734T>C XP_005248319.1:p.Ser912Pro
XM_005248262.3:c.2887T>C XP_005248319.2:p.Ser963Pro
XM_011513990.1:c.2779T>C XP_011512292.1:p.Ser927Pro
XM_017009177.1:c.2887T>C XP_016864666.1:p.Ser963Pro
XM_017009178.1:c.1792T>C XP_016864667.1:p.Ser598Pro
XM_017009179.2:c.1792T>C XP_016864668.1:p.Ser598Pro
XM_017009180.1:c.2887T>C XP_016864669.1:p.Ser963Pro
XM_017009181.1:c.2887T>C XP_016864670.1:p.Ser963Pro
XM_017009182.1:c.2887T>C XP_016864671.1:p.Ser963Pro
XM_017009183.1:c.2887T>C XP_016864672.1:p.Ser963Pro
XM_017009184.1:c.2887T>C XP_016864673.1:p.Ser963Pro
XM_017009187.1:c.2887T>C XP_016864676.1:p.Ser963Pro
XM_024454388.1:c.1792T>C XP_024310156.1:p.Ser598Pro
XM_024454389.1:c.1381T>C XP_024310157.1:p.Ser461Pro
XR_001742034.1:n.2904T>C
XR_001742035.1:n.2904T>C
XR_925598.1:n.2986T>C