Canonical Allele Identifier: CA3204318

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 1157787
• ClinVar RCV Id: RCV001500943 ; RCV004546662
• dbSNP Id: rs375299394
• ExAC: 5:13876889 G / A
• gnomAD v2: 5-13876889-G-A
• gnomAD v3: 5-13876780-G-A
• gnomAD v4: 5-13876780-G-A
• MyVariant Identifiers: chr5:g.13876889G>A (hg19) ; chr5:g.13876780G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13876780G>A , CM000667.2:g.13876780G>A	GRCh38
NC_000005.9:g.13876889G>A , CM000667.1:g.13876889G>A	GRCh37
NC_000005.8:g.13929889G>A	NCBI36
NG_013081.1:g.72701C>T
NG_013081.2:g.72701C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3300C>T MANE Select	ENSP00000265104.4:p.Pro1100=
ENST00000681290.1:c.3255C>T	ENSP00000505288.1:p.Pro1085=
ENST00000265104.4:c.3300C>T	ENSP00000265104.4:p.Pro1100=
NM_001369.2:c.3300C>T	NP_001360.1:p.Pro1100=
XM_005248262.2:c.3255C>T	XP_005248319.1:p.Pro1085=
XM_011513990.1:c.3300C>T	XP_011512292.1:p.Pro1100=
XR_925598.1:n.3507C>T
XM_005248262.3:c.3408C>T	XP_005248319.2:p.Pro1136=
XM_017009177.1:c.3408C>T	XP_016864666.1:p.Pro1136=
XM_017009178.1:c.2313C>T	XP_016864667.1:p.Pro771=
XM_017009179.2:c.2313C>T	XP_016864668.1:p.Pro771=
XM_017009180.1:c.3408C>T	XP_016864669.1:p.Pro1136=
XM_017009181.1:c.3408C>T	XP_016864670.1:p.Pro1136=
XM_017009182.1:c.3408C>T	XP_016864671.1:p.Pro1136=
XM_017009183.1:c.3408C>T	XP_016864672.1:p.Pro1136=
XM_017009184.1:c.3408C>T	XP_016864673.1:p.Pro1136=
XM_017009187.1:c.3408C>T	XP_016864676.1:p.Pro1136=
XM_024454388.1:c.2313C>T	XP_024310156.1:p.Pro771=
XM_024454389.1:c.1902C>T	XP_024310157.1:p.Pro634=
XR_001742034.1:n.3425C>T
XR_001742035.1:n.3425C>T
NM_001369.3:c.3300C>T MANE Select	NP_001360.1:p.Pro1100=