Canonical Allele Identifier: CA1363365805
Gene: KLHDC8B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49173316C= , CM000665.2:g.49173316C= GRCh38
NC_000003.11:g.49210749C= , CM000665.1:g.49210749C= GRCh37
NC_000003.10:g.49185753C= NCBI36
NG_027702.1:g.6732C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000332780.4:c.376+171C= MANE Select ENSP00000327468.2:n.376+171C=
ENST00000332780.3:c.376+171C= ENSP00000327468.2:n.376+171C=
ENST00000459846.6:n.230+515C=
ENST00000476495.2:n.463+141C=
NM_173546.2:c.376+171C= NP_775817.1:n.376+171C=
XM_005264938.1:c.376+171C= XP_005264995.1:n.376+171C=
XM_005264939.3:c.-6+515C= XP_005264996.1:n.-6+515C=
XM_005264940.3:c.-6+515C= XP_005264997.1:n.-6+515C=
XM_006713015.1:c.406+141C= XP_006713078.1:n.406+141C=
XM_006713016.1:c.406+141C= XP_006713079.1:n.406+141C=
XM_005264938.3:c.376+171C= XP_005264995.1:n.376+171C=
XM_005264940.4:c.-6+515C= XP_005264997.1:n.-6+515C=
XM_006713015.3:c.406+141C= XP_006713078.1:n.406+141C=
XM_006713016.3:c.406+141C= XP_006713079.1:n.406+141C=
NM_173546.3:c.376+171C= MANE Select NP_775817.1:n.376+171C=