Canonical Allele Identifier: CA819531788

Gene: PEX7

Linked Data

• dbSNP Id: rs1294595953
• gnomAD v4: 6-136866800-G-T
• MyVariant Identifiers: chr6:g.137187938G>T (hg19) ; chr6:g.136866800G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866800G>T , CM000668.2:g.136866800G>T	GRCh38
NC_000006.11:g.137187938G>T , CM000668.1:g.137187938G>T	GRCh37
NC_000006.10:g.137229631G>T	NCBI36
NG_008462.1:g.49221G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.633+67G>T MANE Select	ENSP00000315680.3:n.633+67G>T
ENST00000541292.6:c.633+67G>T	ENSP00000441004.1:n.633+67G>T
ENST00000678002.1:c.321+67G>T
ENST00000678557.1:c.519+67G>T	ENSP00000502962.1:n.519+67G>T
ENST00000678593.1:c.638+67G>T	ENSP00000503841.1:n.638+67G>T
ENST00000679286.1:c.513+67G>T	ENSP00000503168.1:n.513+67G>T
ENST00000318471.4:c.633+67G>T	ENSP00000315680.3:n.633+67G>T
ENST00000541292.5:c.633+67G>T	ENSP00000441004.1:n.633+67G>T
NM_000288.3:c.633+67G>T	NP_000279.1:n.633+67G>T
XM_005267019.3:c.519+67G>T	XP_005267076.1:n.519+67G>T
XM_006715502.1:c.340-3090G>T	XP_006715565.1:n.340-3090G>T
XM_011535900.1:c.526+20619G>T	XP_011534202.1:n.526+20619G>T
XM_005267019.4:c.519+67G>T	XP_005267076.1:n.519+67G>T
XM_006715502.2:c.340-3090G>T	XP_006715565.1:n.340-3090G>T
XM_017010934.2:c.526+20619G>T	XP_016866423.1:n.526+20619G>T
NM_000288.4:c.633+67G>T MANE Select	NP_000279.1:n.633+67G>T