Canonical Allele Identifier: CA2581632306

Gene: PHF10

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.169713148C= , CM000668.2:g.169713148C=	GRCh38
NC_000006.11:g.170113244C= , CM000668.1:g.170113244C=	GRCh37
NC_000006.10:g.169855169C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339209.9:c.804-609G= MANE Select	ENSP00000341805.4:n.804-609G=
ENST00000339209.8:c.804-609G=	ENSP00000341805.4:n.804-609G=
ENST00000366780.8:c.798-609G=	ENSP00000355743.4:n.798-609G=
ENST00000480008.1:n.768-609G=
ENST00000612128.1:c.804-609G=	ENSP00000479515.1:n.804-609G=
ENST00000621772.4:c.663-609G=	ENSP00000484117.1:n.663-609G=
NM_018288.3:c.804-609G=	NP_060758.2:n.804-609G=
NM_133325.2:c.798-609G=	NP_579866.2:n.798-609G=
NM_018288.4:c.804-609G= MANE Select	NP_060758.2:n.804-609G=
NM_133325.3:c.798-609G=	NP_579866.2:n.798-609G=