Canonical Allele Identifier: CA359201973

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13769170C>G (hg19) ; chr5:g.13769061C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769061C>G , CM000667.2:g.13769061C>G	GRCh38
NC_000005.9:g.13769170C>G , CM000667.1:g.13769170C>G	GRCh37
NC_000005.8:g.13822170C>G	NCBI36
NG_013081.1:g.180420G>C
NG_013081.2:g.180420G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.9796G>C MANE Select	ENSP00000265104.4:p.Ala3266Pro
ENST00000681290.1:c.9751G>C	ENSP00000505288.1:p.Ala3251Pro
ENST00000265104.4:c.9796G>C	ENSP00000265104.4:p.Ala3266Pro
ENST00000504001.3:n.508G>C
NM_001369.2:c.9796G>C	NP_001360.1:p.Ala3266Pro
XM_005248262.2:c.9751G>C	XP_005248319.1:p.Ala3251Pro
XM_005248262.3:c.9904G>C	XP_005248319.2:p.Ala3302Pro
XM_017009177.1:c.9904G>C	XP_016864666.1:p.Ala3302Pro
XM_017009178.1:c.8809G>C	XP_016864667.1:p.Ala2937Pro
XM_017009179.2:c.8809G>C	XP_016864668.1:p.Ala2937Pro
XM_017009180.1:c.9904G>C	XP_016864669.1:p.Ala3302Pro
XM_017009181.1:c.9904G>C	XP_016864670.1:p.Ala3302Pro
XM_017009182.1:c.9904G>C	XP_016864671.1:p.Ala3302Pro
XM_017009185.1:c.4993G>C	XP_016864674.1:p.Ala1665Pro
XM_017009186.1:c.4546G>C	XP_016864675.1:p.Ala1516Pro
XM_017009188.1:c.3883G>C	XP_016864677.1:p.Ala1295Pro
XM_024454388.1:c.8809G>C	XP_024310156.1:p.Ala2937Pro
XM_024454389.1:c.8398G>C	XP_024310157.1:p.Ala2800Pro
NM_001369.3:c.9796G>C MANE Select	NP_001360.1:p.Ala3266Pro