Canonical Allele Identifier: CA359207225

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13717513A>C (hg19) ; chr5:g.13717404A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717404A>C , CM000667.2:g.13717404A>C	GRCh38
NC_000005.9:g.13717513A>C , CM000667.1:g.13717513A>C	GRCh37
NC_000005.8:g.13770513A>C	NCBI36
NG_013081.1:g.232077T>G
NG_013081.2:g.232077T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.12616T>G MANE Select	ENSP00000265104.4:p.Trp4206Gly
ENST00000681290.1:c.12571T>G	ENSP00000505288.1:p.Trp4191Gly
ENST00000265104.4:c.12616T>G	ENSP00000265104.4:p.Trp4206Gly
NM_001369.2:c.12616T>G	NP_001360.1:p.Trp4206Gly
XM_005248262.2:c.12571T>G	XP_005248319.1:p.Trp4191Gly
XM_005248262.3:c.12724T>G	XP_005248319.2:p.Trp4242Gly
XM_017009177.1:c.12724T>G	XP_016864666.1:p.Trp4242Gly
XM_017009178.1:c.11629T>G	XP_016864667.1:p.Trp3877Gly
XM_017009179.2:c.11629T>G	XP_016864668.1:p.Trp3877Gly
XM_017009180.1:c.12724T>G	XP_016864669.1:p.Trp4242Gly
XM_017009185.1:c.7813T>G	XP_016864674.1:p.Trp2605Gly
XM_017009186.1:c.7366T>G	XP_016864675.1:p.Trp2456Gly
XM_017009188.1:c.6703T>G	XP_016864677.1:p.Trp2235Gly
XM_024454388.1:c.11629T>G	XP_024310156.1:p.Trp3877Gly
XM_024454389.1:c.11218T>G	XP_024310157.1:p.Trp3740Gly
NM_001369.3:c.12616T>G MANE Select	NP_001360.1:p.Trp4206Gly