Canonical Allele Identifier: CA365855265
Gene: PEX7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822735T>A , CM000668.2:g.136822735T>A GRCh38
NC_000006.11:g.137143873T>A , CM000668.1:g.137143873T>A GRCh37
NC_000006.10:g.137185566T>A NCBI36
NG_008462.1:g.5156T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318471.5:c.70T>A MANE Select ENSP00000315680.3:p.Phe24Ile
ENST00000541292.6:c.70T>A ENSP00000441004.1:p.Phe24Ile
ENST00000678593.1:c.70T>A ENSP00000503841.1:p.Phe24Ile
ENST00000318471.4:c.70T>A ENSP00000315680.3:p.Phe24Ile
ENST00000367756.8:c.70T>A ENSP00000356730.4:p.Phe24Ile
ENST00000541292.5:c.70T>A ENSP00000441004.1:p.Phe24Ile
NM_000288.3:c.70T>A NP_000279.1:p.Phe24Ile
XM_006715502.1:c.70T>A XP_006715565.1:p.Phe24Ile
XM_011535900.1:c.70T>A XP_011534202.1:p.Phe24Ile
XM_006715502.2:c.70T>A XP_006715565.1:p.Phe24Ile
XM_017010934.2:c.70T>A XP_016866423.1:p.Phe24Ile
NM_000288.4:c.70T>A MANE Select NP_000279.1:p.Phe24Ile