Canonical Allele Identifier: CA359204174

Gene: DNAH5

Linked Data

• dbSNP Id: rs1561215004
• MyVariant Identifiers: chr5:g.13770880C>T (hg19) ; chr5:g.13770771C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770771C>T , CM000667.2:g.13770771C>T	GRCh38
NC_000005.9:g.13770880C>T , CM000667.1:g.13770880C>T	GRCh37
NC_000005.8:g.13823880C>T	NCBI36
NG_013081.1:g.178710G>A
NG_013081.2:g.178710G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9583G>A MANE Select	ENSP00000265104.4:p.Glu3195Lys
ENST00000681290.1:c.9538G>A	ENSP00000505288.1:p.Glu3180Lys
ENST00000265104.4:c.9583G>A	ENSP00000265104.4:p.Glu3195Lys
ENST00000504001.3:n.295G>A
NM_001369.2:c.9583G>A	NP_001360.1:p.Glu3195Lys
XM_005248262.2:c.9538G>A	XP_005248319.1:p.Glu3180Lys
XM_005248262.3:c.9691G>A	XP_005248319.2:p.Glu3231Lys
XM_017009177.1:c.9691G>A	XP_016864666.1:p.Glu3231Lys
XM_017009178.1:c.8596G>A	XP_016864667.1:p.Glu2866Lys
XM_017009179.2:c.8596G>A	XP_016864668.1:p.Glu2866Lys
XM_017009180.1:c.9691G>A	XP_016864669.1:p.Glu3231Lys
XM_017009181.1:c.9691G>A	XP_016864670.1:p.Glu3231Lys
XM_017009182.1:c.9691G>A	XP_016864671.1:p.Glu3231Lys
XM_017009183.1:c.9691G>A	XP_016864672.1:p.Glu3231Lys
XM_017009185.1:c.4780G>A	XP_016864674.1:p.Glu1594Lys
XM_017009186.1:c.4333G>A	XP_016864675.1:p.Glu1445Lys
XM_017009188.1:c.3670G>A	XP_016864677.1:p.Glu1224Lys
XM_024454388.1:c.8596G>A	XP_024310156.1:p.Glu2866Lys
XM_024454389.1:c.8185G>A	XP_024310157.1:p.Glu2729Lys
NM_001369.3:c.9583G>A MANE Select	NP_001360.1:p.Glu3195Lys