Canonical Allele Identifier: CA359207952

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776572A>C (hg19) ; chr5:g.13776463A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776463A>C , CM000667.2:g.13776463A>C	GRCh38
NC_000005.9:g.13776572A>C , CM000667.1:g.13776572A>C	GRCh37
NC_000005.8:g.13829572A>C	NCBI36
NG_013081.1:g.173018T>G
NG_013081.2:g.173018T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9349T>G MANE Select	ENSP00000265104.4:p.Trp3117Gly
ENST00000681290.1:c.9304T>G	ENSP00000505288.1:p.Trp3102Gly
ENST00000265104.4:c.9349T>G	ENSP00000265104.4:p.Trp3117Gly
NM_001369.2:c.9349T>G	NP_001360.1:p.Trp3117Gly
XM_005248262.2:c.9304T>G	XP_005248319.1:p.Trp3102Gly
XM_005248262.3:c.9457T>G	XP_005248319.2:p.Trp3153Gly
XM_017009177.1:c.9457T>G	XP_016864666.1:p.Trp3153Gly
XM_017009178.1:c.8362T>G	XP_016864667.1:p.Trp2788Gly
XM_017009179.2:c.8362T>G	XP_016864668.1:p.Trp2788Gly
XM_017009180.1:c.9457T>G	XP_016864669.1:p.Trp3153Gly
XM_017009181.1:c.9457T>G	XP_016864670.1:p.Trp3153Gly
XM_017009182.1:c.9457T>G	XP_016864671.1:p.Trp3153Gly
XM_017009183.1:c.9457T>G	XP_016864672.1:p.Trp3153Gly
XM_017009185.1:c.4546T>G	XP_016864674.1:p.Trp1516Gly
XM_017009186.1:c.4099T>G	XP_016864675.1:p.Trp1367Gly
XM_017009188.1:c.3436T>G	XP_016864677.1:p.Trp1146Gly
XM_024454388.1:c.8362T>G	XP_024310156.1:p.Trp2788Gly
XM_024454389.1:c.7951T>G	XP_024310157.1:p.Trp2651Gly
NM_001369.3:c.9349T>G MANE Select	NP_001360.1:p.Trp3117Gly