Canonical Allele Identifier: CA1773202678

Gene: PNOC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28324231T= , CM000670.2:g.28324231T=	GRCh38
NC_000008.10:g.28181748T= , CM000670.1:g.28181748T=	GRCh37
NC_000008.9:g.28237667T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301908.8:c.-23-4904T= MANE Select	ENSP00000301908.3:n.-23-4904T=
ENST00000301908.7:c.-23-4904T=	ENSP00000301908.3:n.-23-4904T=
ENST00000518479.5:c.-23-4904T=	ENSP00000428059.1:n.-23-4904T=
NM_006228.4:c.-23-4904T=	NP_006219.1:n.-23-4904T=
XM_005273532.1:c.-23-4904T=	XP_005273589.1:n.-23-4904T=
XM_011544559.1:c.-23-4904T=	XP_011542861.1:n.-23-4904T=
XM_005273532.2:c.-23-4904T=	XP_005273589.1:n.-23-4904T=
XM_011544559.2:c.-23-4904T=	XP_011542861.1:n.-23-4904T=
NM_006228.5:c.-23-4904T= MANE Select	NP_006219.1:n.-23-4904T=