Canonical Allele Identifier: CA2713185422

Gene: PEX7

Linked Data

• dbSNP Id: rs1775201085

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136872474C>G , CM000668.2:g.136872474C>G	GRCh38
NC_000006.11:g.137193612C>G , CM000668.1:g.137193612C>G	GRCh37
NC_000006.10:g.137235305C>G	NCBI36
NG_008462.1:g.54895C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.803+221C>G MANE Select	ENSP00000315680.3:n.803+221C>G
ENST00000541292.6:c.*68+221C>G	ENSP00000441004.1:n.*68+221C>G
ENST00000678002.1:c.491+221C>G
ENST00000678557.1:c.689+221C>G	ENSP00000502962.1:n.689+221C>G
ENST00000678593.1:c.1029C>G	ENSP00000503841.1:n.1029C>G
ENST00000679286.1:c.683+221C>G	ENSP00000503168.1:n.683+221C>G
ENST00000318471.4:c.803+221C>G	ENSP00000315680.3:n.803+221C>G
NM_000288.3:c.803+221C>G	NP_000279.1:n.803+221C>G
XM_005267019.3:c.689+221C>G	XP_005267076.1:n.689+221C>G
XM_006715502.1:c.509+221C>G	XP_006715565.1:n.509+221C>G
XM_011535900.1:c.527-25668C>G	XP_011534202.1:n.527-25668C>G
XM_005267019.4:c.689+221C>G	XP_005267076.1:n.689+221C>G
XM_006715502.2:c.509+221C>G	XP_006715565.1:n.509+221C>G
XM_017010934.2:c.527-25668C>G	XP_016866423.1:n.527-25668C>G
NM_000288.4:c.803+221C>G MANE Select	NP_000279.1:n.803+221C>G