Canonical Allele Identifier: CA359221744

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13793935-C-G
• MyVariant Identifiers: chr5:g.13794044C>G (hg19) ; chr5:g.13793935C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793935C>G , CM000667.2:g.13793935C>G	GRCh38
NC_000005.9:g.13794044C>G , CM000667.1:g.13794044C>G	GRCh37
NC_000005.8:g.13847044C>G	NCBI36
NG_013081.1:g.155546G>C
NG_013081.2:g.155546G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8010+1G>C MANE Select	ENSP00000265104.4:n.8010+1G>C
ENST00000681290.1:c.7965+1G>C	ENSP00000505288.1:n.7965+1G>C
ENST00000265104.4:c.8010+1G>C	ENSP00000265104.4:n.8010+1G>C
NM_001369.2:c.8010+1G>C	NP_001360.1:n.8010+1G>C
XM_005248262.2:c.7965+1G>C	XP_005248319.1:n.7965+1G>C
XM_011513990.1:c.8010+1G>C	XP_011512292.1:n.8010+1G>C
XR_925598.1:n.8217+1G>C
XM_005248262.3:c.8118+1G>C	XP_005248319.2:n.8118+1G>C
XM_017009177.1:c.8118+1G>C	XP_016864666.1:n.8118+1G>C
XM_017009178.1:c.7023+1G>C	XP_016864667.1:n.7023+1G>C
XM_017009179.2:c.7023+1G>C	XP_016864668.1:n.7023+1G>C
XM_017009180.1:c.8118+1G>C	XP_016864669.1:n.8118+1G>C
XM_017009181.1:c.8118+1G>C	XP_016864670.1:n.8118+1G>C
XM_017009182.1:c.8118+1G>C	XP_016864671.1:n.8118+1G>C
XM_017009183.1:c.8118+1G>C	XP_016864672.1:n.8118+1G>C
XM_017009184.1:c.8118+1G>C	XP_016864673.1:n.8118+1G>C
XM_017009185.1:c.3207+1G>C	XP_016864674.1:n.3207+1G>C
XM_017009186.1:c.2760+1G>C	XP_016864675.1:n.2760+1G>C
XM_017009188.1:c.2097+1G>C	XP_016864677.1:n.2097+1G>C
XM_024454388.1:c.7023+1G>C	XP_024310156.1:n.7023+1G>C
XM_024454389.1:c.6612+1G>C	XP_024310157.1:n.6612+1G>C
XR_001742034.1:n.8135+1G>C
XR_001742035.1:n.8135+1G>C
NM_001369.3:c.8010+1G>C MANE Select	NP_001360.1:n.8010+1G>C