Canonical Allele Identifier: CA359208051

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776581A>C (hg19) ; chr5:g.13776472A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776472A>C , CM000667.2:g.13776472A>C	GRCh38
NC_000005.9:g.13776581A>C , CM000667.1:g.13776581A>C	GRCh37
NC_000005.8:g.13829581A>C	NCBI36
NG_013081.1:g.173009T>G
NG_013081.2:g.173009T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9340T>G MANE Select	ENSP00000265104.4:p.Phe3114Val
ENST00000681290.1:c.9295T>G	ENSP00000505288.1:p.Phe3099Val
ENST00000265104.4:c.9340T>G	ENSP00000265104.4:p.Phe3114Val
NM_001369.2:c.9340T>G	NP_001360.1:p.Phe3114Val
XM_005248262.2:c.9295T>G	XP_005248319.1:p.Phe3099Val
XM_005248262.3:c.9448T>G	XP_005248319.2:p.Phe3150Val
XM_017009177.1:c.9448T>G	XP_016864666.1:p.Phe3150Val
XM_017009178.1:c.8353T>G	XP_016864667.1:p.Phe2785Val
XM_017009179.2:c.8353T>G	XP_016864668.1:p.Phe2785Val
XM_017009180.1:c.9448T>G	XP_016864669.1:p.Phe3150Val
XM_017009181.1:c.9448T>G	XP_016864670.1:p.Phe3150Val
XM_017009182.1:c.9448T>G	XP_016864671.1:p.Phe3150Val
XM_017009183.1:c.9448T>G	XP_016864672.1:p.Phe3150Val
XM_017009185.1:c.4537T>G	XP_016864674.1:p.Phe1513Val
XM_017009186.1:c.4090T>G	XP_016864675.1:p.Phe1364Val
XM_017009188.1:c.3427T>G	XP_016864677.1:p.Phe1143Val
XM_024454388.1:c.8353T>G	XP_024310156.1:p.Phe2785Val
XM_024454389.1:c.7942T>G	XP_024310157.1:p.Phe2648Val
NM_001369.3:c.9340T>G MANE Select	NP_001360.1:p.Phe3114Val