Canonical Allele Identifier: CA359202398

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13769229G>C (hg19) ; chr5:g.13769120G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769120G>C , CM000667.2:g.13769120G>C	GRCh38
NC_000005.9:g.13769229G>C , CM000667.1:g.13769229G>C	GRCh37
NC_000005.8:g.13822229G>C	NCBI36
NG_013081.1:g.180361C>G
NG_013081.2:g.180361C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9737C>G MANE Select	ENSP00000265104.4:p.Thr3246Arg
ENST00000681290.1:c.9692C>G	ENSP00000505288.1:p.Thr3231Arg
ENST00000265104.4:c.9737C>G	ENSP00000265104.4:p.Thr3246Arg
ENST00000504001.3:n.449C>G
NM_001369.2:c.9737C>G	NP_001360.1:p.Thr3246Arg
XM_005248262.2:c.9692C>G	XP_005248319.1:p.Thr3231Arg
XM_005248262.3:c.9845C>G	XP_005248319.2:p.Thr3282Arg
XM_017009177.1:c.9845C>G	XP_016864666.1:p.Thr3282Arg
XM_017009178.1:c.8750C>G	XP_016864667.1:p.Thr2917Arg
XM_017009179.2:c.8750C>G	XP_016864668.1:p.Thr2917Arg
XM_017009180.1:c.9845C>G	XP_016864669.1:p.Thr3282Arg
XM_017009181.1:c.9845C>G	XP_016864670.1:p.Thr3282Arg
XM_017009182.1:c.9845C>G	XP_016864671.1:p.Thr3282Arg
XM_017009185.1:c.4934C>G	XP_016864674.1:p.Thr1645Arg
XM_017009186.1:c.4487C>G	XP_016864675.1:p.Thr1496Arg
XM_017009188.1:c.3824C>G	XP_016864677.1:p.Thr1275Arg
XM_024454388.1:c.8750C>G	XP_024310156.1:p.Thr2917Arg
XM_024454389.1:c.8339C>G	XP_024310157.1:p.Thr2780Arg
NM_001369.3:c.9737C>G MANE Select	NP_001360.1:p.Thr3246Arg