Canonical Allele Identifier: CA113981232

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 454770
• ClinVar RCV Id: RCV000542370 ; RCV000729529
• dbSNP Id: rs769589158
• gnomAD v2: 5-13870918-C-G
• gnomAD v3: 5-13870809-C-G
• gnomAD v4: 5-13870809-C-G
• MyVariant Identifiers: chr5:g.13870918C>G (hg19) ; chr5:g.13870809C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13870809C>G , CM000667.2:g.13870809C>G	GRCh38
NC_000005.9:g.13870918C>G , CM000667.1:g.13870918C>G	GRCh37
NC_000005.8:g.13923918C>G	NCBI36
NG_013081.1:g.78672G>C
NG_013081.2:g.78672G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3792G>C MANE Select	ENSP00000265104.4:p.Arg1264Ser
ENST00000681290.1:c.3747G>C	ENSP00000505288.1:p.Arg1249Ser
ENST00000265104.4:c.3792G>C	ENSP00000265104.4:p.Arg1264Ser
NM_001369.2:c.3792G>C	NP_001360.1:p.Arg1264Ser
XM_005248262.2:c.3747G>C	XP_005248319.1:p.Arg1249Ser
XM_011513990.1:c.3792G>C	XP_011512292.1:p.Arg1264Ser
XR_925598.1:n.3999G>C
XM_005248262.3:c.3900G>C	XP_005248319.2:p.Arg1300Ser
XM_017009177.1:c.3900G>C	XP_016864666.1:p.Arg1300Ser
XM_017009178.1:c.2805G>C	XP_016864667.1:p.Arg935Ser
XM_017009179.2:c.2805G>C	XP_016864668.1:p.Arg935Ser
XM_017009180.1:c.3900G>C	XP_016864669.1:p.Arg1300Ser
XM_017009181.1:c.3900G>C	XP_016864670.1:p.Arg1300Ser
XM_017009182.1:c.3900G>C	XP_016864671.1:p.Arg1300Ser
XM_017009183.1:c.3900G>C	XP_016864672.1:p.Arg1300Ser
XM_017009184.1:c.3900G>C	XP_016864673.1:p.Arg1300Ser
XM_017009187.1:c.3900G>C	XP_016864676.1:p.Arg1300Ser
XM_024454388.1:c.2805G>C	XP_024310156.1:p.Arg935Ser
XM_024454389.1:c.2394G>C	XP_024310157.1:p.Arg798Ser
XR_001742034.1:n.3917G>C
XR_001742035.1:n.3917G>C
NM_001369.3:c.3792G>C MANE Select	NP_001360.1:p.Arg1264Ser