Canonical Allele Identifier: CA3204203

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 2191268
• ClinVar RCV Id: RCV002632721
• dbSNP Id: rs770629081
• ExAC: 5:13871045 T / A
• gnomAD v2: 5-13871045-T-A
• gnomAD v4: 5-13870936-T-A
• MyVariant Identifiers: chr5:g.13871045T>A (hg19) ; chr5:g.13870936T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13870936T>A , CM000667.2:g.13870936T>A	GRCh38
NC_000005.9:g.13871045T>A , CM000667.1:g.13871045T>A	GRCh37
NC_000005.8:g.13924045T>A	NCBI36
NG_013081.1:g.78545A>T
NG_013081.2:g.78545A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3665A>T MANE Select	ENSP00000265104.4:p.Asn1222Ile
ENST00000681290.1:c.3620A>T	ENSP00000505288.1:p.Asn1207Ile
ENST00000265104.4:c.3665A>T	ENSP00000265104.4:p.Asn1222Ile
NM_001369.2:c.3665A>T	NP_001360.1:p.Asn1222Ile
XM_005248262.2:c.3620A>T	XP_005248319.1:p.Asn1207Ile
XM_011513990.1:c.3665A>T	XP_011512292.1:p.Asn1222Ile
XR_925598.1:n.3872A>T
XM_005248262.3:c.3773A>T	XP_005248319.2:p.Asn1258Ile
XM_017009177.1:c.3773A>T	XP_016864666.1:p.Asn1258Ile
XM_017009178.1:c.2678A>T	XP_016864667.1:p.Asn893Ile
XM_017009179.2:c.2678A>T	XP_016864668.1:p.Asn893Ile
XM_017009180.1:c.3773A>T	XP_016864669.1:p.Asn1258Ile
XM_017009181.1:c.3773A>T	XP_016864670.1:p.Asn1258Ile
XM_017009182.1:c.3773A>T	XP_016864671.1:p.Asn1258Ile
XM_017009183.1:c.3773A>T	XP_016864672.1:p.Asn1258Ile
XM_017009184.1:c.3773A>T	XP_016864673.1:p.Asn1258Ile
XM_017009187.1:c.3773A>T	XP_016864676.1:p.Asn1258Ile
XM_024454388.1:c.2678A>T	XP_024310156.1:p.Asn893Ile
XM_024454389.1:c.2267A>T	XP_024310157.1:p.Asn756Ile
XR_001742034.1:n.3790A>T
XR_001742035.1:n.3790A>T
NM_001369.3:c.3665A>T MANE Select	NP_001360.1:p.Asn1222Ile