Canonical Allele Identifier: CA2680490767

Gene: PEX7

Linked Data

• dbSNP Id: rs1322830287
• gnomAD v4: 6-136872331-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136872331A>C , CM000668.2:g.136872331A>C	GRCh38
NC_000006.11:g.137193469A>C , CM000668.1:g.137193469A>C	GRCh37
NC_000006.10:g.137235162A>C	NCBI36
NG_008462.1:g.54752A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.803+78A>C MANE Select	ENSP00000315680.3:n.803+78A>C
ENST00000541292.6:c.*68+78A>C	ENSP00000441004.1:n.*68+78A>C
ENST00000678002.1:c.491+78A>C
ENST00000678557.1:c.689+78A>C	ENSP00000502962.1:n.689+78A>C
ENST00000678593.1:c.886A>C	ENSP00000503841.1:n.886A>C
ENST00000679286.1:c.683+78A>C	ENSP00000503168.1:n.683+78A>C
ENST00000318471.4:c.803+78A>C	ENSP00000315680.3:n.803+78A>C
NM_000288.3:c.803+78A>C	NP_000279.1:n.803+78A>C
XM_005267019.3:c.689+78A>C	XP_005267076.1:n.689+78A>C
XM_006715502.1:c.509+78A>C	XP_006715565.1:n.509+78A>C
XM_011535900.1:c.527-25811A>C	XP_011534202.1:n.527-25811A>C
XM_005267019.4:c.689+78A>C	XP_005267076.1:n.689+78A>C
XM_006715502.2:c.509+78A>C	XP_006715565.1:n.509+78A>C
XM_017010934.2:c.527-25811A>C	XP_016866423.1:n.527-25811A>C
NM_000288.4:c.803+78A>C MANE Select	NP_000279.1:n.803+78A>C