Canonical Allele Identifier: CA359197028

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708327T>G (hg19) ; chr5:g.13708218T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708218T>G , CM000667.2:g.13708218T>G	GRCh38
NC_000005.9:g.13708327T>G , CM000667.1:g.13708327T>G	GRCh37
NC_000005.8:g.13761327T>G	NCBI36
NG_013081.1:g.241263A>C
NG_013081.2:g.241263A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.576A>C
ENST00000265104.5:c.13243A>C MANE Select	ENSP00000265104.4:p.Lys4415Gln
ENST00000681290.1:c.13198A>C	ENSP00000505288.1:p.Lys4400Gln
ENST00000265104.4:c.13243A>C	ENSP00000265104.4:p.Lys4415Gln
NM_001369.2:c.13243A>C	NP_001360.1:p.Lys4415Gln
XM_005248262.2:c.13198A>C	XP_005248319.1:p.Lys4400Gln
XM_005248262.3:c.13351A>C	XP_005248319.2:p.Lys4451Gln
XM_017009177.1:c.12931A>C	XP_016864666.1:p.Lys4311Gln
XM_017009178.1:c.12256A>C	XP_016864667.1:p.Lys4086Gln
XM_017009179.2:c.12256A>C	XP_016864668.1:p.Lys4086Gln
XM_017009185.1:c.8440A>C	XP_016864674.1:p.Lys2814Gln
XM_017009186.1:c.7993A>C	XP_016864675.1:p.Lys2665Gln
XM_017009188.1:c.7330A>C	XP_016864677.1:p.Lys2444Gln
XM_024454388.1:c.12256A>C	XP_024310156.1:p.Lys4086Gln
XM_024454389.1:c.11845A>C	XP_024310157.1:p.Lys3949Gln
NM_001369.3:c.13243A>C MANE Select	NP_001360.1:p.Lys4415Gln