Canonical Allele Identifier: CA359209762

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776796C>G (hg19) ; chr5:g.13776687C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776687C>G , CM000667.2:g.13776687C>G	GRCh38
NC_000005.9:g.13776796C>G , CM000667.1:g.13776796C>G	GRCh37
NC_000005.8:g.13829796C>G	NCBI36
NG_013081.1:g.172794G>C
NG_013081.2:g.172794G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9125G>C MANE Select	ENSP00000265104.4:p.Arg3042Pro
ENST00000681290.1:c.9080G>C	ENSP00000505288.1:p.Arg3027Pro
ENST00000265104.4:c.9125G>C	ENSP00000265104.4:p.Arg3042Pro
NM_001369.2:c.9125G>C	NP_001360.1:p.Arg3042Pro
XM_005248262.2:c.9080G>C	XP_005248319.1:p.Arg3027Pro
XM_011513990.1:c.*12G>C	XP_011512292.1:n.*12G>C
XR_925598.1:n.9196G>C
XM_005248262.3:c.9233G>C	XP_005248319.2:p.Arg3078Pro
XM_017009177.1:c.9233G>C	XP_016864666.1:p.Arg3078Pro
XM_017009178.1:c.8138G>C	XP_016864667.1:p.Arg2713Pro
XM_017009179.2:c.8138G>C	XP_016864668.1:p.Arg2713Pro
XM_017009180.1:c.9233G>C	XP_016864669.1:p.Arg3078Pro
XM_017009181.1:c.9233G>C	XP_016864670.1:p.Arg3078Pro
XM_017009182.1:c.9233G>C	XP_016864671.1:p.Arg3078Pro
XM_017009183.1:c.9233G>C	XP_016864672.1:p.Arg3078Pro
XM_017009184.1:c.*12G>C	XP_016864673.1:n.*12G>C
XM_017009185.1:c.4322G>C	XP_016864674.1:p.Arg1441Pro
XM_017009186.1:c.3875G>C	XP_016864675.1:p.Arg1292Pro
XM_017009188.1:c.3212G>C	XP_016864677.1:p.Arg1071Pro
XM_024454388.1:c.8138G>C	XP_024310156.1:p.Arg2713Pro
XM_024454389.1:c.7727G>C	XP_024310157.1:p.Arg2576Pro
XR_001742034.1:n.9119G>C
XR_001742035.1:n.9114G>C
NM_001369.3:c.9125G>C MANE Select	NP_001360.1:p.Arg3042Pro