Canonical Allele Identifier: CA359208204

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776602A>G (hg19) ; chr5:g.13776493A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776493A>G , CM000667.2:g.13776493A>G	GRCh38
NC_000005.9:g.13776602A>G , CM000667.1:g.13776602A>G	GRCh37
NC_000005.8:g.13829602A>G	NCBI36
NG_013081.1:g.172988T>C
NG_013081.2:g.172988T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9319T>C MANE Select	ENSP00000265104.4:p.Ser3107Pro
ENST00000681290.1:c.9274T>C	ENSP00000505288.1:p.Ser3092Pro
ENST00000265104.4:c.9319T>C	ENSP00000265104.4:p.Ser3107Pro
NM_001369.2:c.9319T>C	NP_001360.1:p.Ser3107Pro
XM_005248262.2:c.9274T>C	XP_005248319.1:p.Ser3092Pro
XM_005248262.3:c.9427T>C	XP_005248319.2:p.Ser3143Pro
XM_017009177.1:c.9427T>C	XP_016864666.1:p.Ser3143Pro
XM_017009178.1:c.8332T>C	XP_016864667.1:p.Ser2778Pro
XM_017009179.2:c.8332T>C	XP_016864668.1:p.Ser2778Pro
XM_017009180.1:c.9427T>C	XP_016864669.1:p.Ser3143Pro
XM_017009181.1:c.9427T>C	XP_016864670.1:p.Ser3143Pro
XM_017009182.1:c.9427T>C	XP_016864671.1:p.Ser3143Pro
XM_017009183.1:c.9427T>C	XP_016864672.1:p.Ser3143Pro
XM_017009185.1:c.4516T>C	XP_016864674.1:p.Ser1506Pro
XM_017009186.1:c.4069T>C	XP_016864675.1:p.Ser1357Pro
XM_017009188.1:c.3406T>C	XP_016864677.1:p.Ser1136Pro
XM_024454388.1:c.8332T>C	XP_024310156.1:p.Ser2778Pro
XM_024454389.1:c.7921T>C	XP_024310157.1:p.Ser2641Pro
NM_001369.3:c.9319T>C MANE Select	NP_001360.1:p.Ser3107Pro