Canonical Allele Identifier: CA3201570

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717335C>T , CM000667.2:g.13717335C>T	GRCh38
NC_000005.9:g.13717444C>T , CM000667.1:g.13717444C>T	GRCh37
NC_000005.8:g.13770444C>T	NCBI36
NG_013081.1:g.232146G>A
NG_013081.2:g.232146G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.12685G>A MANE Select	NP_001360.1:p.Asp4229Asn
ENST00000265104.5:c.12685G>A MANE Select	ENSP00000265104.4:p.Asp4229Asn
NM_001369.2:c.12685G>A	NP_001360.1:p.Asp4229Asn
ENST00000265104.4:c.12685G>A	ENSP00000265104.4:p.Asp4229Asn
ENST00000681290.1:c.12640G>A	ENSP00000505288.1:p.Asp4214Asn
XM_005248262.2:c.12640G>A	XP_005248319.1:p.Asp4214Asn
XM_005248262.3:c.12793G>A	XP_005248319.2:p.Asp4265Asn
XM_017009177.1:c.12793G>A	XP_016864666.1:p.Asp4265Asn
XM_017009178.1:c.11698G>A	XP_016864667.1:p.Asp3900Asn
XM_017009179.2:c.11698G>A	XP_016864668.1:p.Asp3900Asn
XM_017009180.1:c.12793G>A	XP_016864669.1:p.Asp4265Asn
XM_017009185.1:c.7882G>A	XP_016864674.1:p.Asp2628Asn
XM_017009186.1:c.7435G>A	XP_016864675.1:p.Asp2479Asn
XM_017009188.1:c.6772G>A	XP_016864677.1:p.Asp2258Asn
XM_024454388.1:c.11698G>A	XP_024310156.1:p.Asp3900Asn
XM_024454389.1:c.11287G>A	XP_024310157.1:p.Asp3763Asn