Canonical Allele Identifier: CA359198088

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708302G>A , CM000667.2:g.13708302G>A	GRCh38
NC_000005.9:g.13708411G>A , CM000667.1:g.13708411G>A	GRCh37
NC_000005.8:g.13761411G>A	NCBI36
NG_013081.1:g.241179C>T
NG_013081.2:g.241179C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.13159C>T MANE Select	NP_001360.1:p.Gln4387Ter
ENST00000265104.5:c.13159C>T MANE Select	ENSP00000265104.4:p.Gln4387Ter
NM_001369.2:c.13159C>T	NP_001360.1:p.Gln4387Ter
ENST00000265104.4:c.13159C>T	ENSP00000265104.4:p.Gln4387Ter
ENST00000681290.1:c.13114C>T	ENSP00000505288.1:p.Gln4372Ter
ENST00000683611.1:n.492C>T
XM_005248262.2:c.13114C>T	XP_005248319.1:p.Gln4372Ter
XM_005248262.3:c.13267C>T	XP_005248319.2:p.Gln4423Ter
XM_017009177.1:c.12847C>T	XP_016864666.1:p.Gln4283Ter
XM_017009178.1:c.12172C>T	XP_016864667.1:p.Gln4058Ter
XM_017009179.2:c.12172C>T	XP_016864668.1:p.Gln4058Ter
XM_017009185.1:c.8356C>T	XP_016864674.1:p.Gln2786Ter
XM_017009186.1:c.7909C>T	XP_016864675.1:p.Gln2637Ter
XM_017009188.1:c.7246C>T	XP_016864677.1:p.Gln2416Ter
XM_024454388.1:c.12172C>T	XP_024310156.1:p.Gln4058Ter
XM_024454389.1:c.11761C>T	XP_024310157.1:p.Gln3921Ter