Canonical Allele Identifier: CA359188603

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13692154G>C (hg19) ; chr5:g.13692045G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692045G>C , CM000667.2:g.13692045G>C	GRCh38
NC_000005.9:g.13692154G>C , CM000667.1:g.13692154G>C	GRCh37
NC_000005.8:g.13745154G>C	NCBI36
NG_013081.1:g.257436C>G
NG_013081.2:g.257436C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1147C>G
ENST00000265104.5:c.13814C>G MANE Select	ENSP00000265104.4:p.Thr4605Arg
ENST00000681290.1:c.13769C>G	ENSP00000505288.1:p.Thr4590Arg
ENST00000265104.4:c.13814C>G	ENSP00000265104.4:p.Thr4605Arg
NM_001369.2:c.13814C>G	NP_001360.1:p.Thr4605Arg
XM_005248262.2:c.13769C>G	XP_005248319.1:p.Thr4590Arg
XM_005248262.3:c.13922C>G	XP_005248319.2:p.Thr4641Arg
XM_017009177.1:c.13502C>G	XP_016864666.1:p.Thr4501Arg
XM_017009178.1:c.12827C>G	XP_016864667.1:p.Thr4276Arg
XM_017009179.2:c.12827C>G	XP_016864668.1:p.Thr4276Arg
XM_017009185.1:c.9011C>G	XP_016864674.1:p.Thr3004Arg
XM_017009186.1:c.8564C>G	XP_016864675.1:p.Thr2855Arg
XM_017009188.1:c.7901C>G	XP_016864677.1:p.Thr2634Arg
XM_024454388.1:c.12827C>G	XP_024310156.1:p.Thr4276Arg
XM_024454389.1:c.12416C>G	XP_024310157.1:p.Thr4139Arg
NM_001369.3:c.13814C>G MANE Select	NP_001360.1:p.Thr4605Arg