Canonical Allele Identifier: CA359213094

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13721128A>G (hg19) ; chr5:g.13721019A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13721019A>G , CM000667.2:g.13721019A>G	GRCh38
NC_000005.9:g.13721128A>G , CM000667.1:g.13721128A>G	GRCh37
NC_000005.8:g.13774128A>G	NCBI36
NG_013081.1:g.228462T>C
NG_013081.2:g.228462T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.12260T>C MANE Select	ENSP00000265104.4:p.Leu4087Ser
ENST00000681290.1:c.12215T>C	ENSP00000505288.1:p.Leu4072Ser
ENST00000265104.4:c.12260T>C	ENSP00000265104.4:p.Leu4087Ser
NM_001369.2:c.12260T>C	NP_001360.1:p.Leu4087Ser
XM_005248262.2:c.12215T>C	XP_005248319.1:p.Leu4072Ser
XM_005248262.3:c.12368T>C	XP_005248319.2:p.Leu4123Ser
XM_017009177.1:c.12368T>C	XP_016864666.1:p.Leu4123Ser
XM_017009178.1:c.11273T>C	XP_016864667.1:p.Leu3758Ser
XM_017009179.2:c.11273T>C	XP_016864668.1:p.Leu3758Ser
XM_017009180.1:c.12368T>C	XP_016864669.1:p.Leu4123Ser
XM_017009185.1:c.7457T>C	XP_016864674.1:p.Leu2486Ser
XM_017009186.1:c.7010T>C	XP_016864675.1:p.Leu2337Ser
XM_017009188.1:c.6347T>C	XP_016864677.1:p.Leu2116Ser
XM_024454388.1:c.11273T>C	XP_024310156.1:p.Leu3758Ser
XM_024454389.1:c.10862T>C	XP_024310157.1:p.Leu3621Ser
NM_001369.3:c.12260T>C MANE Select	NP_001360.1:p.Leu4087Ser