Canonical Allele Identifier: CA8396351
Gene: DNAH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11747740A>G , CM000679.2:g.11747740A>G GRCh38
NC_000017.10:g.11651057A>G , CM000679.1:g.11651057A>G GRCh37
NC_000017.9:g.11591782A>G NCBI36
NG_047047.1:g.154310A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001372.4:c.6584A>G MANE Select NP_001363.2:p.Asn2195Ser
ENST00000262442.9:c.6584A>G MANE Select ENSP00000262442.3:p.Asn2195Ser
NM_001372.3:c.6584A>G NP_001363.2:p.Asn2195Ser
ENST00000262442.8:c.6584A>G ENSP00000262442.3:p.Asn2195Ser
ENST00000454412.6:c.6584A>G ENSP00000414874.2:p.Asn2195Ser
XM_011523703.1:c.6584A>G XP_011522005.1:p.Asn2195Ser
XM_011523703.2:c.6584A>G XP_011522005.1:p.Asn2195Ser
XM_017024292.2:c.6467A>G XP_016879781.1:p.Asn2156Ser
XM_017024293.1:c.4466A>G XP_016879782.1:p.Asn1489Ser
XM_017024294.2:c.6584A>G XP_016879783.1:p.Asn2195Ser
XM_017024295.2:c.6584A>G XP_016879784.1:p.Asn2195Ser