Canonical Allele Identifier: CA359192611

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13701443A>C (hg19) ; chr5:g.13701334A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13701334A>C , CM000667.2:g.13701334A>C	GRCh38
NC_000005.9:g.13701443A>C , CM000667.1:g.13701443A>C	GRCh37
NC_000005.8:g.13754443A>C	NCBI36
NG_013081.1:g.248147T>G
NG_013081.2:g.248147T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.774T>G
ENST00000265104.5:c.13441T>G MANE Select	ENSP00000265104.4:p.Trp4481Gly
ENST00000681290.1:c.13396T>G	ENSP00000505288.1:p.Trp4466Gly
ENST00000265104.4:c.13441T>G	ENSP00000265104.4:p.Trp4481Gly
NM_001369.2:c.13441T>G	NP_001360.1:p.Trp4481Gly
XM_005248262.2:c.13396T>G	XP_005248319.1:p.Trp4466Gly
XM_005248262.3:c.13549T>G	XP_005248319.2:p.Trp4517Gly
XM_017009177.1:c.13129T>G	XP_016864666.1:p.Trp4377Gly
XM_017009178.1:c.12454T>G	XP_016864667.1:p.Trp4152Gly
XM_017009179.2:c.12454T>G	XP_016864668.1:p.Trp4152Gly
XM_017009185.1:c.8638T>G	XP_016864674.1:p.Trp2880Gly
XM_017009186.1:c.8191T>G	XP_016864675.1:p.Trp2731Gly
XM_017009188.1:c.7528T>G	XP_016864677.1:p.Trp2510Gly
XM_024454388.1:c.12454T>G	XP_024310156.1:p.Trp4152Gly
XM_024454389.1:c.12043T>G	XP_024310157.1:p.Trp4015Gly
NM_001369.3:c.13441T>G MANE Select	NP_001360.1:p.Trp4481Gly