Canonical Allele Identifier: CA443535617

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13770971A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770862A>G , CM000667.2:g.13770862A>G	GRCh38
NC_000005.9:g.13770971A>G , CM000667.1:g.13770971A>G	GRCh37
NC_000005.8:g.13823971A>G	NCBI36
NG_013081.1:g.178619T>C
NG_013081.2:g.178619T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9492T>C MANE Select	ENSP00000265104.4:p.Phe3164=
ENST00000681290.1:c.9447T>C	ENSP00000505288.1:p.Phe3149=
ENST00000265104.4:c.9492T>C	ENSP00000265104.4:p.Phe3164=
ENST00000504001.3:n.204T>C
NM_001369.2:c.9492T>C	NP_001360.1:p.Phe3164=
XM_005248262.2:c.9447T>C	XP_005248319.1:p.Phe3149=
XM_005248262.3:c.9600T>C	XP_005248319.2:p.Phe3200=
XM_017009177.1:c.9600T>C	XP_016864666.1:p.Phe3200=
XM_017009178.1:c.8505T>C	XP_016864667.1:p.Phe2835=
XM_017009179.2:c.8505T>C	XP_016864668.1:p.Phe2835=
XM_017009180.1:c.9600T>C	XP_016864669.1:p.Phe3200=
XM_017009181.1:c.9600T>C	XP_016864670.1:p.Phe3200=
XM_017009182.1:c.9600T>C	XP_016864671.1:p.Phe3200=
XM_017009183.1:c.9600T>C	XP_016864672.1:p.Phe3200=
XM_017009185.1:c.4689T>C	XP_016864674.1:p.Phe1563=
XM_017009186.1:c.4242T>C	XP_016864675.1:p.Phe1414=
XM_017009188.1:c.3579T>C	XP_016864677.1:p.Phe1193=
XM_024454388.1:c.8505T>C	XP_024310156.1:p.Phe2835=
XM_024454389.1:c.8094T>C	XP_024310157.1:p.Phe2698=
NM_001369.3:c.9492T>C MANE Select	NP_001360.1:p.Phe3164=