Canonical Allele Identifier: CA443251256

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708337G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708228G>C , CM000667.2:g.13708228G>C	GRCh38
NC_000005.9:g.13708337G>C , CM000667.1:g.13708337G>C	GRCh37
NC_000005.8:g.13761337G>C	NCBI36
NG_013081.1:g.241253C>G
NG_013081.2:g.241253C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.566C>G
ENST00000265104.5:c.13233C>G MANE Select	ENSP00000265104.4:p.Leu4411=
ENST00000681290.1:c.13188C>G	ENSP00000505288.1:p.Leu4396=
ENST00000265104.4:c.13233C>G	ENSP00000265104.4:p.Leu4411=
NM_001369.2:c.13233C>G	NP_001360.1:p.Leu4411=
XM_005248262.2:c.13188C>G	XP_005248319.1:p.Leu4396=
XM_005248262.3:c.13341C>G	XP_005248319.2:p.Leu4447=
XM_017009177.1:c.12921C>G	XP_016864666.1:p.Leu4307=
XM_017009178.1:c.12246C>G	XP_016864667.1:p.Leu4082=
XM_017009179.2:c.12246C>G	XP_016864668.1:p.Leu4082=
XM_017009185.1:c.8430C>G	XP_016864674.1:p.Leu2810=
XM_017009186.1:c.7983C>G	XP_016864675.1:p.Leu2661=
XM_017009188.1:c.7320C>G	XP_016864677.1:p.Leu2440=
XM_024454388.1:c.12246C>G	XP_024310156.1:p.Leu4082=
XM_024454389.1:c.11835C>G	XP_024310157.1:p.Leu3945=
NM_001369.3:c.13233C>G MANE Select	NP_001360.1:p.Leu4411=