Canonical Allele Identifier: CA359207498

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13717533C>A (hg19) ; chr5:g.13717424C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717424C>A , CM000667.2:g.13717424C>A	GRCh38
NC_000005.9:g.13717533C>A , CM000667.1:g.13717533C>A	GRCh37
NC_000005.8:g.13770533C>A	NCBI36
NG_013081.1:g.232057G>T
NG_013081.2:g.232057G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.12596G>T MANE Select	ENSP00000265104.4:p.Arg4199Leu
ENST00000681290.1:c.12551G>T	ENSP00000505288.1:p.Arg4184Leu
ENST00000265104.4:c.12596G>T	ENSP00000265104.4:p.Arg4199Leu
NM_001369.2:c.12596G>T	NP_001360.1:p.Arg4199Leu
XM_005248262.2:c.12551G>T	XP_005248319.1:p.Arg4184Leu
XM_005248262.3:c.12704G>T	XP_005248319.2:p.Arg4235Leu
XM_017009177.1:c.12704G>T	XP_016864666.1:p.Arg4235Leu
XM_017009178.1:c.11609G>T	XP_016864667.1:p.Arg3870Leu
XM_017009179.2:c.11609G>T	XP_016864668.1:p.Arg3870Leu
XM_017009180.1:c.12704G>T	XP_016864669.1:p.Arg4235Leu
XM_017009185.1:c.7793G>T	XP_016864674.1:p.Arg2598Leu
XM_017009186.1:c.7346G>T	XP_016864675.1:p.Arg2449Leu
XM_017009188.1:c.6683G>T	XP_016864677.1:p.Arg2228Leu
XM_024454388.1:c.11609G>T	XP_024310156.1:p.Arg3870Leu
XM_024454389.1:c.11198G>T	XP_024310157.1:p.Arg3733Leu
NM_001369.3:c.12596G>T MANE Select	NP_001360.1:p.Arg4199Leu