Canonical Allele Identifier: CA152167186

Gene: PHF10

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.169723861C>T , CM000668.2:g.169723861C>T	GRCh38
NC_000006.11:g.170123957C>T , CM000668.1:g.170123957C>T	GRCh37
NC_000006.10:g.169865882C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018288.4:c.71G>A MANE Select	NP_060758.2:p.Gly24Glu
ENST00000339209.9:c.71G>A MANE Select	ENSP00000341805.4:p.Gly24Glu
NM_018288.3:c.71G>A	NP_060758.2:p.Gly24Glu
NM_133325.2:c.71G>A	NP_579866.2:p.Gly24Glu
NM_133325.3:c.71G>A	NP_579866.2:p.Gly24Glu
ENST00000339209.8:c.71G>A	ENSP00000341805.4:p.Gly24Glu
ENST00000366780.8:c.71G>A	ENSP00000355743.4:p.Gly24Glu
ENST00000480008.1:n.145G>A
ENST00000612128.1:c.71G>A	ENSP00000479515.1:p.Gly24Glu
ENST00000621772.4:c.-55+1560G>A	ENSP00000484117.1:n.-55+1560G>A