Canonical Allele Identifier: CA1528462543

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13839128_13839129delinsCA , CM000667.2:g.13839128_13839129delinsCA	GRCh38
NC_000005.9:g.13839237_13839238delinsCA , CM000667.1:g.13839237_13839238delinsCA	GRCh37
NC_000005.8:g.13892237_13892238delinsCA	NCBI36
NG_013081.1:g.110352_110353delinsTG
NG_013081.2:g.110352_110353delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.5882+227_5882+228delinsTG MANE Select	ENSP00000265104.4:n.5882+227_5882+228deli...
ENST00000681290.1:c.5837+227_5837+228delinsTG	ENSP00000505288.1:n.5837+227_5837+228deli...
ENST00000265104.4:c.5882+227_5882+228delinsTG	ENSP00000265104.4:n.5882+227_5882+228deli...
NM_001369.2:c.5882+227_5882+228delinsTG	NP_001360.1:n.5882+227_5882+228delinsTG
XM_005248262.2:c.5837+227_5837+228delinsTG	XP_005248319.1:n.5837+227_5837+228delinsT...
XM_011513990.1:c.5882+227_5882+228delinsTG	XP_011512292.1:n.5882+227_5882+228delinsT...
XR_925598.1:n.6089+227_6089+228delinsTG
XM_005248262.3:c.5990+227_5990+228delinsTG	XP_005248319.2:n.5990+227_5990+228delinsT...
XM_017009177.1:c.5990+227_5990+228delinsTG	XP_016864666.1:n.5990+227_5990+228delinsT...
XM_017009178.1:c.4895+227_4895+228delinsTG	XP_016864667.1:n.4895+227_4895+228delinsT...
XM_017009179.2:c.4895+227_4895+228delinsTG	XP_016864668.1:n.4895+227_4895+228delinsT...
XM_017009180.1:c.5990+227_5990+228delinsTG	XP_016864669.1:n.5990+227_5990+228delinsT...
XM_017009181.1:c.5990+227_5990+228delinsTG	XP_016864670.1:n.5990+227_5990+228delinsT...
XM_017009182.1:c.5990+227_5990+228delinsTG	XP_016864671.1:n.5990+227_5990+228delinsT...
XM_017009183.1:c.5990+227_5990+228delinsTG	XP_016864672.1:n.5990+227_5990+228delinsT...
XM_017009184.1:c.5990+227_5990+228delinsTG	XP_016864673.1:n.5990+227_5990+228delinsT...
XM_017009185.1:c.1079+227_1079+228delinsTG	XP_016864674.1:n.1079+227_1079+228delinsT...
XM_017009186.1:c.632+227_632+228delinsTG	XP_016864675.1:n.632+227_632+228delinsTG
XM_017009187.1:c.5990+227_5990+228delinsTG	XP_016864676.1:n.5990+227_5990+228delinsT...
XM_024454388.1:c.4895+227_4895+228delinsTG	XP_024310156.1:n.4895+227_4895+228delinsT...
XM_024454389.1:c.4484+227_4484+228delinsTG	XP_024310157.1:n.4484+227_4484+228delinsT...
XR_001742034.1:n.6007+227_6007+228delinsTG
XR_001742035.1:n.6007+227_6007+228delinsTG
NM_001369.3:c.5882+227_5882+228delinsTG MANE Select	NP_001360.1:n.5882+227_5882+228delinsTG