Canonical Allele Identifier: CA365764478

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137193381T>G (hg19) ; chr6:g.136872243T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136872243T>G , CM000668.2:g.136872243T>G	GRCh38
NC_000006.11:g.137193381T>G , CM000668.1:g.137193381T>G	GRCh37
NC_000006.10:g.137235074T>G	NCBI36
NG_008462.1:g.54664T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.793T>G MANE Select	ENSP00000315680.3:p.Phe265Val
ENST00000541292.6:c.*58T>G	ENSP00000441004.1:n.*58T>G
ENST00000678002.1:c.481T>G
ENST00000678557.1:c.679T>G	ENSP00000502962.1:p.Phe227Val
ENST00000678593.1:c.798T>G	ENSP00000503841.1:n.798T>G
ENST00000679286.1:c.673T>G	ENSP00000503168.1:p.Phe225Val
ENST00000318471.4:c.793T>G	ENSP00000315680.3:p.Phe265Val
NM_000288.3:c.793T>G	NP_000279.1:p.Phe265Val
XM_005267019.3:c.679T>G	XP_005267076.1:p.Phe227Val
XM_006715502.1:c.499T>G	XP_006715565.1:p.Phe167Val
XM_011535900.1:c.527-25899T>G	XP_011534202.1:n.527-25899T>G
XM_005267019.4:c.679T>G	XP_005267076.1:p.Phe227Val
XM_006715502.2:c.499T>G	XP_006715565.1:p.Phe167Val
XM_017010934.2:c.527-25899T>G	XP_016866423.1:n.527-25899T>G
NM_000288.4:c.793T>G MANE Select	NP_000279.1:p.Phe265Val