Canonical Allele Identifier: CA359196212

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708122C>G , CM000667.2:g.13708122C>G	GRCh38
NC_000005.9:g.13708231C>G , CM000667.1:g.13708231C>G	GRCh37
NC_000005.8:g.13761231C>G	NCBI36
NG_013081.1:g.241359G>C
NG_013081.2:g.241359G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.13338+1G>C MANE Select	NP_001360.1:n.13338+1G>C
ENST00000265104.5:c.13338+1G>C MANE Select	ENSP00000265104.4:n.13338+1G>C
NM_001369.2:c.13338+1G>C	NP_001360.1:n.13338+1G>C
ENST00000265104.4:c.13338+1G>C	ENSP00000265104.4:n.13338+1G>C
ENST00000681290.1:c.13293+1G>C	ENSP00000505288.1:n.13293+1G>C
ENST00000683611.1:n.671+1G>C
XM_005248262.2:c.13293+1G>C	XP_005248319.1:n.13293+1G>C
XM_005248262.3:c.13446+1G>C	XP_005248319.2:n.13446+1G>C
XM_017009177.1:c.13026+1G>C	XP_016864666.1:n.13026+1G>C
XM_017009178.1:c.12351+1G>C	XP_016864667.1:n.12351+1G>C
XM_017009179.2:c.12351+1G>C	XP_016864668.1:n.12351+1G>C
XM_017009185.1:c.8535+1G>C	XP_016864674.1:n.8535+1G>C
XM_017009186.1:c.8088+1G>C	XP_016864675.1:n.8088+1G>C
XM_017009188.1:c.7425+1G>C	XP_016864677.1:n.7425+1G>C
XM_024454388.1:c.12351+1G>C	XP_024310156.1:n.12351+1G>C
XM_024454389.1:c.11940+1G>C	XP_024310157.1:n.11940+1G>C