Canonical Allele Identifier: CA359209304

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776740G>T (hg19) ; chr5:g.13776631G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776631G>T , CM000667.2:g.13776631G>T	GRCh38
NC_000005.9:g.13776740G>T , CM000667.1:g.13776740G>T	GRCh37
NC_000005.8:g.13829740G>T	NCBI36
NG_013081.1:g.172850C>A
NG_013081.2:g.172850C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9181C>A MANE Select	ENSP00000265104.4:p.Pro3061Thr
ENST00000681290.1:c.9136C>A	ENSP00000505288.1:p.Pro3046Thr
ENST00000265104.4:c.9181C>A	ENSP00000265104.4:p.Pro3061Thr
NM_001369.2:c.9181C>A	NP_001360.1:p.Pro3061Thr
XM_005248262.2:c.9136C>A	XP_005248319.1:p.Pro3046Thr
XM_005248262.3:c.9289C>A	XP_005248319.2:p.Pro3097Thr
XM_017009177.1:c.9289C>A	XP_016864666.1:p.Pro3097Thr
XM_017009178.1:c.8194C>A	XP_016864667.1:p.Pro2732Thr
XM_017009179.2:c.8194C>A	XP_016864668.1:p.Pro2732Thr
XM_017009180.1:c.9289C>A	XP_016864669.1:p.Pro3097Thr
XM_017009181.1:c.9289C>A	XP_016864670.1:p.Pro3097Thr
XM_017009182.1:c.9289C>A	XP_016864671.1:p.Pro3097Thr
XM_017009183.1:c.9289C>A	XP_016864672.1:p.Pro3097Thr
XM_017009184.1:c.*68C>A	XP_016864673.1:n.*68C>A
XM_017009185.1:c.4378C>A	XP_016864674.1:p.Pro1460Thr
XM_017009186.1:c.3931C>A	XP_016864675.1:p.Pro1311Thr
XM_017009188.1:c.3268C>A	XP_016864677.1:p.Pro1090Thr
XM_024454388.1:c.8194C>A	XP_024310156.1:p.Pro2732Thr
XM_024454389.1:c.7783C>A	XP_024310157.1:p.Pro2595Thr
XR_001742034.1:n.9175C>A
XR_001742035.1:n.9170C>A
NM_001369.3:c.9181C>A MANE Select	NP_001360.1:p.Pro3061Thr