Canonical Allele Identifier: CA359196935

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708312C>G (hg19) ; chr5:g.13708203C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708203C>G , CM000667.2:g.13708203C>G	GRCh38
NC_000005.9:g.13708312C>G , CM000667.1:g.13708312C>G	GRCh37
NC_000005.8:g.13761312C>G	NCBI36
NG_013081.1:g.241278G>C
NG_013081.2:g.241278G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.591G>C
ENST00000265104.5:c.13258G>C MANE Select	ENSP00000265104.4:p.Gly4420Arg
ENST00000681290.1:c.13213G>C	ENSP00000505288.1:p.Gly4405Arg
ENST00000265104.4:c.13258G>C	ENSP00000265104.4:p.Gly4420Arg
NM_001369.2:c.13258G>C	NP_001360.1:p.Gly4420Arg
XM_005248262.2:c.13213G>C	XP_005248319.1:p.Gly4405Arg
XM_005248262.3:c.13366G>C	XP_005248319.2:p.Gly4456Arg
XM_017009177.1:c.12946G>C	XP_016864666.1:p.Gly4316Arg
XM_017009178.1:c.12271G>C	XP_016864667.1:p.Gly4091Arg
XM_017009179.2:c.12271G>C	XP_016864668.1:p.Gly4091Arg
XM_017009185.1:c.8455G>C	XP_016864674.1:p.Gly2819Arg
XM_017009186.1:c.8008G>C	XP_016864675.1:p.Gly2670Arg
XM_017009188.1:c.7345G>C	XP_016864677.1:p.Gly2449Arg
XM_024454388.1:c.12271G>C	XP_024310156.1:p.Gly4091Arg
XM_024454389.1:c.11860G>C	XP_024310157.1:p.Gly3954Arg
NM_001369.3:c.13258G>C MANE Select	NP_001360.1:p.Gly4420Arg