Canonical Allele Identifier: CA359202410

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13769232A>C (hg19) ; chr5:g.13769123A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769123A>C , CM000667.2:g.13769123A>C	GRCh38
NC_000005.9:g.13769232A>C , CM000667.1:g.13769232A>C	GRCh37
NC_000005.8:g.13822232A>C	NCBI36
NG_013081.1:g.180358T>G
NG_013081.2:g.180358T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9734T>G MANE Select	ENSP00000265104.4:p.Val3245Gly
ENST00000681290.1:c.9689T>G	ENSP00000505288.1:p.Val3230Gly
ENST00000265104.4:c.9734T>G	ENSP00000265104.4:p.Val3245Gly
ENST00000504001.3:n.446T>G
NM_001369.2:c.9734T>G	NP_001360.1:p.Val3245Gly
XM_005248262.2:c.9689T>G	XP_005248319.1:p.Val3230Gly
XM_005248262.3:c.9842T>G	XP_005248319.2:p.Val3281Gly
XM_017009177.1:c.9842T>G	XP_016864666.1:p.Val3281Gly
XM_017009178.1:c.8747T>G	XP_016864667.1:p.Val2916Gly
XM_017009179.2:c.8747T>G	XP_016864668.1:p.Val2916Gly
XM_017009180.1:c.9842T>G	XP_016864669.1:p.Val3281Gly
XM_017009181.1:c.9842T>G	XP_016864670.1:p.Val3281Gly
XM_017009182.1:c.9842T>G	XP_016864671.1:p.Val3281Gly
XM_017009185.1:c.4931T>G	XP_016864674.1:p.Val1644Gly
XM_017009186.1:c.4484T>G	XP_016864675.1:p.Val1495Gly
XM_017009188.1:c.3821T>G	XP_016864677.1:p.Val1274Gly
XM_024454388.1:c.8747T>G	XP_024310156.1:p.Val2916Gly
XM_024454389.1:c.8336T>G	XP_024310157.1:p.Val2779Gly
NM_001369.3:c.9734T>G MANE Select	NP_001360.1:p.Val3245Gly