Canonical Allele Identifier: CA359223119

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13735323A>G (hg19) ; chr5:g.13735214A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735214A>G , CM000667.2:g.13735214A>G	GRCh38
NC_000005.9:g.13735323A>G , CM000667.1:g.13735323A>G	GRCh37
NC_000005.8:g.13788323A>G	NCBI36
NG_013081.1:g.214267T>C
NG_013081.2:g.214267T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.11678T>C MANE Select	ENSP00000265104.4:p.Phe3893Ser
ENST00000681290.1:c.11633T>C	ENSP00000505288.1:p.Phe3878Ser
ENST00000265104.4:c.11678T>C	ENSP00000265104.4:p.Phe3893Ser
NM_001369.2:c.11678T>C	NP_001360.1:p.Phe3893Ser
XM_005248262.2:c.11633T>C	XP_005248319.1:p.Phe3878Ser
XM_005248262.3:c.11786T>C	XP_005248319.2:p.Phe3929Ser
XM_017009177.1:c.11786T>C	XP_016864666.1:p.Phe3929Ser
XM_017009178.1:c.10691T>C	XP_016864667.1:p.Phe3564Ser
XM_017009179.2:c.10691T>C	XP_016864668.1:p.Phe3564Ser
XM_017009180.1:c.11786T>C	XP_016864669.1:p.Phe3929Ser
XM_017009181.1:c.11786T>C	XP_016864670.1:p.Phe3929Ser
XM_017009185.1:c.6875T>C	XP_016864674.1:p.Phe2292Ser
XM_017009186.1:c.6428T>C	XP_016864675.1:p.Phe2143Ser
XM_017009188.1:c.5765T>C	XP_016864677.1:p.Phe1922Ser
XM_024454388.1:c.10691T>C	XP_024310156.1:p.Phe3564Ser
XM_024454389.1:c.10280T>C	XP_024310157.1:p.Phe3427Ser
NM_001369.3:c.11678T>C MANE Select	NP_001360.1:p.Phe3893Ser