Canonical Allele Identifier: CA359208410

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13717617T>A (hg19) ; chr5:g.13717508T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717508T>A , CM000667.2:g.13717508T>A	GRCh38
NC_000005.9:g.13717617T>A , CM000667.1:g.13717617T>A	GRCh37
NC_000005.8:g.13770617T>A	NCBI36
NG_013081.1:g.231973A>T
NG_013081.2:g.231973A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.12512A>T MANE Select	ENSP00000265104.4:p.Asp4171Val
ENST00000681290.1:c.12467A>T	ENSP00000505288.1:p.Asp4156Val
ENST00000265104.4:c.12512A>T	ENSP00000265104.4:p.Asp4171Val
NM_001369.2:c.12512A>T	NP_001360.1:p.Asp4171Val
XM_005248262.2:c.12467A>T	XP_005248319.1:p.Asp4156Val
XM_005248262.3:c.12620A>T	XP_005248319.2:p.Asp4207Val
XM_017009177.1:c.12620A>T	XP_016864666.1:p.Asp4207Val
XM_017009178.1:c.11525A>T	XP_016864667.1:p.Asp3842Val
XM_017009179.2:c.11525A>T	XP_016864668.1:p.Asp3842Val
XM_017009180.1:c.12620A>T	XP_016864669.1:p.Asp4207Val
XM_017009185.1:c.7709A>T	XP_016864674.1:p.Asp2570Val
XM_017009186.1:c.7262A>T	XP_016864675.1:p.Asp2421Val
XM_017009188.1:c.6599A>T	XP_016864677.1:p.Asp2200Val
XM_024454388.1:c.11525A>T	XP_024310156.1:p.Asp3842Val
XM_024454389.1:c.11114A>T	XP_024310157.1:p.Asp3705Val
NM_001369.3:c.12512A>T MANE Select	NP_001360.1:p.Asp4171Val