Canonical Allele Identifier: CA359207449

Gene: DNAH5

Linked Data

• COSMIC: COSM1204088
• MyVariant Identifiers: chr5:g.13717530T>C (hg19) ; chr5:g.13717421T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717421T>C , CM000667.2:g.13717421T>C	GRCh38
NC_000005.9:g.13717530T>C , CM000667.1:g.13717530T>C	GRCh37
NC_000005.8:g.13770530T>C	NCBI36
NG_013081.1:g.232060A>G
NG_013081.2:g.232060A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.12599A>G MANE Select	ENSP00000265104.4:p.Lys4200Arg
ENST00000681290.1:c.12554A>G	ENSP00000505288.1:p.Lys4185Arg
ENST00000265104.4:c.12599A>G	ENSP00000265104.4:p.Lys4200Arg
NM_001369.2:c.12599A>G	NP_001360.1:p.Lys4200Arg
XM_005248262.2:c.12554A>G	XP_005248319.1:p.Lys4185Arg
XM_005248262.3:c.12707A>G	XP_005248319.2:p.Lys4236Arg
XM_017009177.1:c.12707A>G	XP_016864666.1:p.Lys4236Arg
XM_017009178.1:c.11612A>G	XP_016864667.1:p.Lys3871Arg
XM_017009179.2:c.11612A>G	XP_016864668.1:p.Lys3871Arg
XM_017009180.1:c.12707A>G	XP_016864669.1:p.Lys4236Arg
XM_017009185.1:c.7796A>G	XP_016864674.1:p.Lys2599Arg
XM_017009186.1:c.7349A>G	XP_016864675.1:p.Lys2450Arg
XM_017009188.1:c.6686A>G	XP_016864677.1:p.Lys2229Arg
XM_024454388.1:c.11612A>G	XP_024310156.1:p.Lys3871Arg
XM_024454389.1:c.11201A>G	XP_024310157.1:p.Lys3734Arg
NM_001369.3:c.12599A>G MANE Select	NP_001360.1:p.Lys4200Arg