Canonical Allele Identifier: CA12398598

Gene: PHF10

Genomic Alleles

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

Transcript Alleles

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