Canonical Allele Identifier: CA359191998

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13753562T>G (hg19) ; chr5:g.13753453T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753453T>G , CM000667.2:g.13753453T>G	GRCh38
NC_000005.9:g.13753562T>G , CM000667.1:g.13753562T>G	GRCh37
NC_000005.8:g.13806562T>G	NCBI36
NG_013081.1:g.196028A>C
NG_013081.2:g.196028A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10652A>C MANE Select	ENSP00000265104.4:p.Lys3551Thr
ENST00000681290.1:c.10607A>C	ENSP00000505288.1:p.Lys3536Thr
ENST00000265104.4:c.10652A>C	ENSP00000265104.4:p.Lys3551Thr
NM_001369.2:c.10652A>C	NP_001360.1:p.Lys3551Thr
XM_005248262.2:c.10607A>C	XP_005248319.1:p.Lys3536Thr
XM_005248262.3:c.10760A>C	XP_005248319.2:p.Lys3587Thr
XM_017009177.1:c.10760A>C	XP_016864666.1:p.Lys3587Thr
XM_017009178.1:c.9665A>C	XP_016864667.1:p.Lys3222Thr
XM_017009179.2:c.9665A>C	XP_016864668.1:p.Lys3222Thr
XM_017009180.1:c.10760A>C	XP_016864669.1:p.Lys3587Thr
XM_017009181.1:c.10760A>C	XP_016864670.1:p.Lys3587Thr
XM_017009182.1:c.10760A>C	XP_016864671.1:p.Lys3587Thr
XM_017009185.1:c.5849A>C	XP_016864674.1:p.Lys1950Thr
XM_017009186.1:c.5402A>C	XP_016864675.1:p.Lys1801Thr
XM_017009188.1:c.4739A>C	XP_016864677.1:p.Lys1580Thr
XM_024454388.1:c.9665A>C	XP_024310156.1:p.Lys3222Thr
XM_024454389.1:c.9254A>C	XP_024310157.1:p.Lys3085Thr
NM_001369.3:c.10652A>C MANE Select	NP_001360.1:p.Lys3551Thr