Canonical Allele Identifier: CA359220832

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13793636C>G (hg19) ; chr5:g.13793527C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793527C>G , CM000667.2:g.13793527C>G	GRCh38
NC_000005.9:g.13793636C>G , CM000667.1:g.13793636C>G	GRCh37
NC_000005.8:g.13846636C>G	NCBI36
NG_013081.1:g.155954G>C
NG_013081.2:g.155954G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8212G>C MANE Select	ENSP00000265104.4:p.Asp2738His
ENST00000681290.1:c.8167G>C	ENSP00000505288.1:p.Asp2723His
ENST00000265104.4:c.8212G>C	ENSP00000265104.4:p.Asp2738His
NM_001369.2:c.8212G>C	NP_001360.1:p.Asp2738His
XM_005248262.2:c.8167G>C	XP_005248319.1:p.Asp2723His
XM_011513990.1:c.8212G>C	XP_011512292.1:p.Asp2738His
XR_925598.1:n.8419G>C
XM_005248262.3:c.8320G>C	XP_005248319.2:p.Asp2774His
XM_017009177.1:c.8320G>C	XP_016864666.1:p.Asp2774His
XM_017009178.1:c.7225G>C	XP_016864667.1:p.Asp2409His
XM_017009179.2:c.7225G>C	XP_016864668.1:p.Asp2409His
XM_017009180.1:c.8320G>C	XP_016864669.1:p.Asp2774His
XM_017009181.1:c.8320G>C	XP_016864670.1:p.Asp2774His
XM_017009182.1:c.8320G>C	XP_016864671.1:p.Asp2774His
XM_017009183.1:c.8320G>C	XP_016864672.1:p.Asp2774His
XM_017009184.1:c.8320G>C	XP_016864673.1:p.Asp2774His
XM_017009185.1:c.3409G>C	XP_016864674.1:p.Asp1137His
XM_017009186.1:c.2962G>C	XP_016864675.1:p.Asp988His
XM_017009188.1:c.2299G>C	XP_016864677.1:p.Asp767His
XM_024454388.1:c.7225G>C	XP_024310156.1:p.Asp2409His
XM_024454389.1:c.6814G>C	XP_024310157.1:p.Asp2272His
XR_001742034.1:n.8337G>C
XR_001742035.1:n.8337G>C
NM_001369.3:c.8212G>C MANE Select	NP_001360.1:p.Asp2738His