Canonical Allele Identifier: CA359198887

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13891093T>C (hg19) ; chr5:g.13890984T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13890984T>C , CM000667.2:g.13890984T>C	GRCh38
NC_000005.9:g.13891093T>C , CM000667.1:g.13891093T>C	GRCh37
NC_000005.8:g.13944093T>C	NCBI36
NG_013081.1:g.58497A>G
NG_013081.2:g.58497A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.2569A>G MANE Select	ENSP00000265104.4:p.Met857Val
ENST00000681290.1:c.2524A>G	ENSP00000505288.1:p.Met842Val
ENST00000265104.4:c.2569A>G	ENSP00000265104.4:p.Met857Val
NM_001369.2:c.2569A>G	NP_001360.1:p.Met857Val
XM_005248262.2:c.2524A>G	XP_005248319.1:p.Met842Val
XM_011513990.1:c.2569A>G	XP_011512292.1:p.Met857Val
XR_925598.1:n.2776A>G
XM_005248262.3:c.2677A>G	XP_005248319.2:p.Met893Val
XM_017009177.1:c.2677A>G	XP_016864666.1:p.Met893Val
XM_017009178.1:c.1582A>G	XP_016864667.1:p.Met528Val
XM_017009179.2:c.1582A>G	XP_016864668.1:p.Met528Val
XM_017009180.1:c.2677A>G	XP_016864669.1:p.Met893Val
XM_017009181.1:c.2677A>G	XP_016864670.1:p.Met893Val
XM_017009182.1:c.2677A>G	XP_016864671.1:p.Met893Val
XM_017009183.1:c.2677A>G	XP_016864672.1:p.Met893Val
XM_017009184.1:c.2677A>G	XP_016864673.1:p.Met893Val
XM_017009187.1:c.2677A>G	XP_016864676.1:p.Met893Val
XM_024454388.1:c.1582A>G	XP_024310156.1:p.Met528Val
XM_024454389.1:c.1171A>G	XP_024310157.1:p.Met391Val
XR_001742034.1:n.2694A>G
XR_001742035.1:n.2694A>G
NM_001369.3:c.2569A>G MANE Select	NP_001360.1:p.Met857Val