Canonical Allele Identifier: CA443535666

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776567G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776458G>C , CM000667.2:g.13776458G>C	GRCh38
NC_000005.9:g.13776567G>C , CM000667.1:g.13776567G>C	GRCh37
NC_000005.8:g.13829567G>C	NCBI36
NG_013081.1:g.173023C>G
NG_013081.2:g.173023C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9354C>G MANE Select	ENSP00000265104.4:p.Pro3118=
ENST00000681290.1:c.9309C>G	ENSP00000505288.1:p.Pro3103=
ENST00000265104.4:c.9354C>G	ENSP00000265104.4:p.Pro3118=
NM_001369.2:c.9354C>G	NP_001360.1:p.Pro3118=
XM_005248262.2:c.9309C>G	XP_005248319.1:p.Pro3103=
XM_005248262.3:c.9462C>G	XP_005248319.2:p.Pro3154=
XM_017009177.1:c.9462C>G	XP_016864666.1:p.Pro3154=
XM_017009178.1:c.8367C>G	XP_016864667.1:p.Pro2789=
XM_017009179.2:c.8367C>G	XP_016864668.1:p.Pro2789=
XM_017009180.1:c.9462C>G	XP_016864669.1:p.Pro3154=
XM_017009181.1:c.9462C>G	XP_016864670.1:p.Pro3154=
XM_017009182.1:c.9462C>G	XP_016864671.1:p.Pro3154=
XM_017009183.1:c.9462C>G	XP_016864672.1:p.Pro3154=
XM_017009185.1:c.4551C>G	XP_016864674.1:p.Pro1517=
XM_017009186.1:c.4104C>G	XP_016864675.1:p.Pro1368=
XM_017009188.1:c.3441C>G	XP_016864677.1:p.Pro1147=
XM_024454388.1:c.8367C>G	XP_024310156.1:p.Pro2789=
XM_024454389.1:c.7956C>G	XP_024310157.1:p.Pro2652=
NM_001369.3:c.9354C>G MANE Select	NP_001360.1:p.Pro3118=