Canonical Allele Identifier: CA359211931

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13911437C>G , CM000667.2:g.13911437C>G	GRCh38
NC_000005.9:g.13911546C>G , CM000667.1:g.13911546C>G	GRCh37
NC_000005.8:g.13964546C>G	NCBI36
NG_013081.1:g.38044G>C
NG_013081.2:g.38044G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.1593G>C MANE Select	NP_001360.1:p.Met531Ile
ENST00000265104.5:c.1593G>C MANE Select	ENSP00000265104.4:p.Met531Ile
NM_001369.2:c.1593G>C	NP_001360.1:p.Met531Ile
ENST00000265104.4:c.1593G>C	ENSP00000265104.4:p.Met531Ile
ENST00000508040.1:n.2001G>C
ENST00000680213.1:c.1353G>C	ENSP00000506622.1:p.Met451Ile
ENST00000680213.2:n.1649G>C
ENST00000681290.1:c.1548G>C	ENSP00000505288.1:p.Met516Ile
ENST00000683011.1:n.1532G>C
ENST00000683967.1:n.3958G>C
ENST00000684013.1:n.2253G>C
ENST00000684099.1:n.2249G>C
XM_005248262.2:c.1548G>C	XP_005248319.1:p.Met516Ile
XM_005248262.3:c.1701G>C	XP_005248319.2:p.Met567Ile
XM_011513990.1:c.1593G>C	XP_011512292.1:p.Met531Ile
XM_017009177.1:c.1701G>C	XP_016864666.1:p.Met567Ile
XM_017009178.1:c.606G>C	XP_016864667.1:p.Met202Ile
XM_017009179.2:c.606G>C	XP_016864668.1:p.Met202Ile
XM_017009180.1:c.1701G>C	XP_016864669.1:p.Met567Ile
XM_017009181.1:c.1701G>C	XP_016864670.1:p.Met567Ile
XM_017009182.1:c.1701G>C	XP_016864671.1:p.Met567Ile
XM_017009183.1:c.1701G>C	XP_016864672.1:p.Met567Ile
XM_017009184.1:c.1701G>C	XP_016864673.1:p.Met567Ile
XM_017009187.1:c.1701G>C	XP_016864676.1:p.Met567Ile
XM_024454388.1:c.606G>C	XP_024310156.1:p.Met202Ile
XM_024454389.1:c.195G>C	XP_024310157.1:p.Met65Ile
XR_001742034.1:n.1718G>C
XR_001742035.1:n.1718G>C
XR_925598.1:n.1800G>C