Canonical Allele Identifier: CA365766561

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219296A>C (hg19) ; chr6:g.136898158A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898158A>C , CM000668.2:g.136898158A>C	GRCh38
NC_000006.11:g.137219296A>C , CM000668.1:g.137219296A>C	GRCh37
NC_000006.10:g.137260989A>C	NCBI36
NG_008462.1:g.80579A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.820A>C MANE Select	ENSP00000315680.3:p.Lys274Gln
ENST00000541292.6:c.*85A>C	ENSP00000441004.1:n.*85A>C
ENST00000678002.1:c.508A>C
ENST00000678557.1:c.706A>C	ENSP00000502962.1:p.Lys236Gln
ENST00000679286.1:c.700A>C	ENSP00000503168.1:p.Lys234Gln
ENST00000318471.4:c.820A>C	ENSP00000315680.3:p.Lys274Gln
NM_000288.3:c.820A>C	NP_000279.1:p.Lys274Gln
XM_005267019.3:c.706A>C	XP_005267076.1:p.Lys236Gln
XM_006715502.1:c.526A>C	XP_006715565.1:p.Lys176Gln
XM_011535900.1:c.543A>C	XP_011534202.1:p.Gln181His
XM_005267019.4:c.706A>C	XP_005267076.1:p.Lys236Gln
XM_006715502.2:c.526A>C	XP_006715565.1:p.Lys176Gln
XM_017010934.2:c.543A>C	XP_016866423.1:p.Gln181His
NM_000288.4:c.820A>C MANE Select	NP_000279.1:p.Lys274Gln