Canonical Allele Identifier: CA359224976

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13736000T>C (hg19) ; chr5:g.13735891T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735891T>C , CM000667.2:g.13735891T>C	GRCh38
NC_000005.9:g.13736000T>C , CM000667.1:g.13736000T>C	GRCh37
NC_000005.8:g.13789000T>C	NCBI36
NG_013081.1:g.213590A>G
NG_013081.2:g.213590A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11497A>G MANE Select	ENSP00000265104.4:p.Met3833Val
ENST00000681290.1:c.11452A>G	ENSP00000505288.1:p.Met3818Val
ENST00000265104.4:c.11497A>G	ENSP00000265104.4:p.Met3833Val
NM_001369.2:c.11497A>G	NP_001360.1:p.Met3833Val
XM_005248262.2:c.11452A>G	XP_005248319.1:p.Met3818Val
XM_005248262.3:c.11605A>G	XP_005248319.2:p.Met3869Val
XM_017009177.1:c.11605A>G	XP_016864666.1:p.Met3869Val
XM_017009178.1:c.10510A>G	XP_016864667.1:p.Met3504Val
XM_017009179.2:c.10510A>G	XP_016864668.1:p.Met3504Val
XM_017009180.1:c.11605A>G	XP_016864669.1:p.Met3869Val
XM_017009181.1:c.11605A>G	XP_016864670.1:p.Met3869Val
XM_017009182.1:c.11361A>G	XP_016864671.1:p.Arg3787=
XM_017009185.1:c.6694A>G	XP_016864674.1:p.Met2232Val
XM_017009186.1:c.6247A>G	XP_016864675.1:p.Met2083Val
XM_017009188.1:c.5584A>G	XP_016864677.1:p.Met1862Val
XM_024454388.1:c.10510A>G	XP_024310156.1:p.Met3504Val
XM_024454389.1:c.10099A>G	XP_024310157.1:p.Met3367Val
NM_001369.3:c.11497A>G MANE Select	NP_001360.1:p.Met3833Val