Canonical Allele Identifier: CA359209829

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13776697-G-T
• MyVariant Identifiers: chr5:g.13776806G>T (hg19) ; chr5:g.13776697G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776697G>T , CM000667.2:g.13776697G>T	GRCh38
NC_000005.9:g.13776806G>T , CM000667.1:g.13776806G>T	GRCh37
NC_000005.8:g.13829806G>T	NCBI36
NG_013081.1:g.172784C>A
NG_013081.2:g.172784C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9115C>A MANE Select	ENSP00000265104.4:p.Leu3039Ile
ENST00000681290.1:c.9070C>A	ENSP00000505288.1:p.Leu3024Ile
ENST00000265104.4:c.9115C>A	ENSP00000265104.4:p.Leu3039Ile
NM_001369.2:c.9115C>A	NP_001360.1:p.Leu3039Ile
XM_005248262.2:c.9070C>A	XP_005248319.1:p.Leu3024Ile
XM_011513990.1:c.*2C>A	XP_011512292.1:n.*2C>A
XR_925598.1:n.9186C>A
XM_005248262.3:c.9223C>A	XP_005248319.2:p.Leu3075Ile
XM_017009177.1:c.9223C>A	XP_016864666.1:p.Leu3075Ile
XM_017009178.1:c.8128C>A	XP_016864667.1:p.Leu2710Ile
XM_017009179.2:c.8128C>A	XP_016864668.1:p.Leu2710Ile
XM_017009180.1:c.9223C>A	XP_016864669.1:p.Leu3075Ile
XM_017009181.1:c.9223C>A	XP_016864670.1:p.Leu3075Ile
XM_017009182.1:c.9223C>A	XP_016864671.1:p.Leu3075Ile
XM_017009183.1:c.9223C>A	XP_016864672.1:p.Leu3075Ile
XM_017009184.1:c.*2C>A	XP_016864673.1:n.*2C>A
XM_017009185.1:c.4312C>A	XP_016864674.1:p.Leu1438Ile
XM_017009186.1:c.3865C>A	XP_016864675.1:p.Leu1289Ile
XM_017009188.1:c.3202C>A	XP_016864677.1:p.Leu1068Ile
XM_024454388.1:c.8128C>A	XP_024310156.1:p.Leu2710Ile
XM_024454389.1:c.7717C>A	XP_024310157.1:p.Leu2573Ile
XR_001742034.1:n.9109C>A
XR_001742035.1:n.9104C>A
NM_001369.3:c.9115C>A MANE Select	NP_001360.1:p.Leu3039Ile