Canonical Allele Identifier: CA365766870

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219378A>C (hg19) ; chr6:g.136898240A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898240A>C , CM000668.2:g.136898240A>C	GRCh38
NC_000006.11:g.137219378A>C , CM000668.1:g.137219378A>C	GRCh37
NC_000006.10:g.137261071A>C	NCBI36
NG_008462.1:g.80661A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.902A>C MANE Select	ENSP00000315680.3:p.Gln301Pro
ENST00000541292.6:c.*167A>C	ENSP00000441004.1:n.*167A>C
ENST00000678002.1:c.590A>C
ENST00000678557.1:c.788A>C	ENSP00000502962.1:p.Gln263Pro
ENST00000679286.1:c.782A>C	ENSP00000503168.1:p.Gln261Pro
ENST00000318471.4:c.902A>C	ENSP00000315680.3:p.Gln301Pro
NM_000288.3:c.902A>C	NP_000279.1:p.Gln301Pro
XM_005267019.3:c.788A>C	XP_005267076.1:p.Gln263Pro
XM_006715502.1:c.608A>C	XP_006715565.1:p.Gln203Pro
XM_005267019.4:c.788A>C	XP_005267076.1:p.Gln263Pro
XM_006715502.2:c.608A>C	XP_006715565.1:p.Gln203Pro
XM_017010934.2:c.*25A>C	XP_016866423.1:n.*25A>C
NM_000288.4:c.902A>C MANE Select	NP_000279.1:p.Gln301Pro