Canonical Allele Identifier: CA287980401
Community Standard Title: NM_001372.4(DNAH9):c.11406+1G>T
Gene: DNAH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.11894497G>T , CM000679.2:g.11894497G>T GRCh38
NC_000017.10:g.11797814G>T , CM000679.1:g.11797814G>T GRCh37
NC_000017.9:g.11738539G>T NCBI36
NG_047047.1:g.301067G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001372.4:c.11406+1G>T MANE Select NP_001363.2:n.11406+1G>T
ENST00000262442.9:c.11406+1G>T MANE Select ENSP00000262442.3:n.11406+1G>T
NM_001372.3:c.11406+1G>T NP_001363.2:n.11406+1G>T
NM_004662.2:c.342+1G>T NP_004653.2:n.342+1G>T
ENST00000262442.8:c.11406+1G>T ENSP00000262442.3:n.11406+1G>T
ENST00000396001.6:n.869+1G>T
ENST00000454412.6:c.11406+1G>T ENSP00000414874.2:n.11406+1G>T
ENST00000581682.1:n.687+1G>T
ENST00000608377.5:c.342+1G>T ENSP00000476951.1:n.342+1G>T
XM_011523703.1:c.11406+1G>T XP_011522005.1:n.11406+1G>T
XM_011523703.2:c.11406+1G>T XP_011522005.1:n.11406+1G>T
XM_017024292.2:c.11289+1G>T XP_016879781.1:n.11289+1G>T
XM_017024293.1:c.9288+1G>T XP_016879782.1:n.9288+1G>T