Canonical Allele Identifier: CA1363365724

Gene: KLHDC8B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49173200C= , CM000665.2:g.49173200C=	GRCh38
NC_000003.11:g.49210633C= , CM000665.1:g.49210633C=	GRCh37
NC_000003.10:g.49185637C=	NCBI36
NG_027702.1:g.6616C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000332780.4:c.376+55C= MANE Select	ENSP00000327468.2:n.376+55C=
ENST00000332780.3:c.376+55C=	ENSP00000327468.2:n.376+55C=
ENST00000459846.6:n.230+399C=
ENST00000476495.2:n.463+25C=
NM_173546.2:c.376+55C=	NP_775817.1:n.376+55C=
XM_005264938.1:c.376+55C=	XP_005264995.1:n.376+55C=
XM_005264939.3:c.-6+399C=	XP_005264996.1:n.-6+399C=
XM_005264940.3:c.-6+399C=	XP_005264997.1:n.-6+399C=
XM_006713015.1:c.406+25C=	XP_006713078.1:n.406+25C=
XM_006713016.1:c.406+25C=	XP_006713079.1:n.406+25C=
XM_005264938.3:c.376+55C=	XP_005264995.1:n.376+55C=
XM_005264940.4:c.-6+399C=	XP_005264997.1:n.-6+399C=
XM_006713015.3:c.406+25C=	XP_006713078.1:n.406+25C=
XM_006713016.3:c.406+25C=	XP_006713079.1:n.406+25C=
NM_173546.3:c.376+55C= MANE Select	NP_775817.1:n.376+55C=