Canonical Allele Identifier: CA359192062

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13753577C>T (hg19) ; chr5:g.13753468C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753468C>T , CM000667.2:g.13753468C>T	GRCh38
NC_000005.9:g.13753577C>T , CM000667.1:g.13753577C>T	GRCh37
NC_000005.8:g.13806577C>T	NCBI36
NG_013081.1:g.196013G>A
NG_013081.2:g.196013G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.10637G>A MANE Select	ENSP00000265104.4:p.Trp3546Ter
ENST00000681290.1:c.10592G>A	ENSP00000505288.1:p.Trp3531Ter
ENST00000265104.4:c.10637G>A	ENSP00000265104.4:p.Trp3546Ter
NM_001369.2:c.10637G>A	NP_001360.1:p.Trp3546Ter
XM_005248262.2:c.10592G>A	XP_005248319.1:p.Trp3531Ter
XM_005248262.3:c.10745G>A	XP_005248319.2:p.Trp3582Ter
XM_017009177.1:c.10745G>A	XP_016864666.1:p.Trp3582Ter
XM_017009178.1:c.9650G>A	XP_016864667.1:p.Trp3217Ter
XM_017009179.2:c.9650G>A	XP_016864668.1:p.Trp3217Ter
XM_017009180.1:c.10745G>A	XP_016864669.1:p.Trp3582Ter
XM_017009181.1:c.10745G>A	XP_016864670.1:p.Trp3582Ter
XM_017009182.1:c.10745G>A	XP_016864671.1:p.Trp3582Ter
XM_017009185.1:c.5834G>A	XP_016864674.1:p.Trp1945Ter
XM_017009186.1:c.5387G>A	XP_016864675.1:p.Trp1796Ter
XM_017009188.1:c.4724G>A	XP_016864677.1:p.Trp1575Ter
XM_024454388.1:c.9650G>A	XP_024310156.1:p.Trp3217Ter
XM_024454389.1:c.9239G>A	XP_024310157.1:p.Trp3080Ter
NM_001369.3:c.10637G>A MANE Select	NP_001360.1:p.Trp3546Ter