Canonical Allele Identifier: CA443253836

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13769162G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769053G>C , CM000667.2:g.13769053G>C	GRCh38
NC_000005.9:g.13769162G>C , CM000667.1:g.13769162G>C	GRCh37
NC_000005.8:g.13822162G>C	NCBI36
NG_013081.1:g.180428C>G
NG_013081.2:g.180428C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9804C>G MANE Select	ENSP00000265104.4:p.Ala3268=
ENST00000681290.1:c.9759C>G	ENSP00000505288.1:p.Ala3253=
ENST00000265104.4:c.9804C>G	ENSP00000265104.4:p.Ala3268=
ENST00000504001.3:n.516C>G
NM_001369.2:c.9804C>G	NP_001360.1:p.Ala3268=
XM_005248262.2:c.9759C>G	XP_005248319.1:p.Ala3253=
XM_005248262.3:c.9912C>G	XP_005248319.2:p.Ala3304=
XM_017009177.1:c.9912C>G	XP_016864666.1:p.Ala3304=
XM_017009178.1:c.8817C>G	XP_016864667.1:p.Ala2939=
XM_017009179.2:c.8817C>G	XP_016864668.1:p.Ala2939=
XM_017009180.1:c.9912C>G	XP_016864669.1:p.Ala3304=
XM_017009181.1:c.9912C>G	XP_016864670.1:p.Ala3304=
XM_017009182.1:c.9912C>G	XP_016864671.1:p.Ala3304=
XM_017009185.1:c.5001C>G	XP_016864674.1:p.Ala1667=
XM_017009186.1:c.4554C>G	XP_016864675.1:p.Ala1518=
XM_017009188.1:c.3891C>G	XP_016864677.1:p.Ala1297=
XM_024454388.1:c.8817C>G	XP_024310156.1:p.Ala2939=
XM_024454389.1:c.8406C>G	XP_024310157.1:p.Ala2802=
NM_001369.3:c.9804C>G MANE Select	NP_001360.1:p.Ala3268=