Canonical Allele Identifier: CA359198077

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708409C>G (hg19) ; chr5:g.13708300C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708300C>G , CM000667.2:g.13708300C>G	GRCh38
NC_000005.9:g.13708409C>G , CM000667.1:g.13708409C>G	GRCh37
NC_000005.8:g.13761409C>G	NCBI36
NG_013081.1:g.241181G>C
NG_013081.2:g.241181G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.494G>C
ENST00000265104.5:c.13161G>C MANE Select	ENSP00000265104.4:p.Gln4387His
ENST00000681290.1:c.13116G>C	ENSP00000505288.1:p.Gln4372His
ENST00000265104.4:c.13161G>C	ENSP00000265104.4:p.Gln4387His
NM_001369.2:c.13161G>C	NP_001360.1:p.Gln4387His
XM_005248262.2:c.13116G>C	XP_005248319.1:p.Gln4372His
XM_005248262.3:c.13269G>C	XP_005248319.2:p.Gln4423His
XM_017009177.1:c.12849G>C	XP_016864666.1:p.Gln4283His
XM_017009178.1:c.12174G>C	XP_016864667.1:p.Gln4058His
XM_017009179.2:c.12174G>C	XP_016864668.1:p.Gln4058His
XM_017009185.1:c.8358G>C	XP_016864674.1:p.Gln2786His
XM_017009186.1:c.7911G>C	XP_016864675.1:p.Gln2637His
XM_017009188.1:c.7248G>C	XP_016864677.1:p.Gln2416His
XM_024454388.1:c.12174G>C	XP_024310156.1:p.Gln4058His
XM_024454389.1:c.11763G>C	XP_024310157.1:p.Gln3921His
NM_001369.3:c.13161G>C MANE Select	NP_001360.1:p.Gln4387His