Canonical Allele Identifier: CA359197347

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708357T>C (hg19) ; chr5:g.13708248T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708248T>C , CM000667.2:g.13708248T>C	GRCh38
NC_000005.9:g.13708357T>C , CM000667.1:g.13708357T>C	GRCh37
NC_000005.8:g.13761357T>C	NCBI36
NG_013081.1:g.241233A>G
NG_013081.2:g.241233A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000683611.1:n.546A>G
ENST00000265104.5:c.13213A>G MANE Select	ENSP00000265104.4:p.Ser4405Gly
ENST00000681290.1:c.13168A>G	ENSP00000505288.1:p.Ser4390Gly
ENST00000265104.4:c.13213A>G	ENSP00000265104.4:p.Ser4405Gly
NM_001369.2:c.13213A>G	NP_001360.1:p.Ser4405Gly
XM_005248262.2:c.13168A>G	XP_005248319.1:p.Ser4390Gly
XM_005248262.3:c.13321A>G	XP_005248319.2:p.Ser4441Gly
XM_017009177.1:c.12901A>G	XP_016864666.1:p.Ser4301Gly
XM_017009178.1:c.12226A>G	XP_016864667.1:p.Ser4076Gly
XM_017009179.2:c.12226A>G	XP_016864668.1:p.Ser4076Gly
XM_017009185.1:c.8410A>G	XP_016864674.1:p.Ser2804Gly
XM_017009186.1:c.7963A>G	XP_016864675.1:p.Ser2655Gly
XM_017009188.1:c.7300A>G	XP_016864677.1:p.Ser2434Gly
XM_024454388.1:c.12226A>G	XP_024310156.1:p.Ser4076Gly
XM_024454389.1:c.11815A>G	XP_024310157.1:p.Ser3939Gly
NM_001369.3:c.13213A>G MANE Select	NP_001360.1:p.Ser4405Gly