Canonical Allele Identifier: CA365766548

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219290T>C (hg19) ; chr6:g.136898152T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898152T>C , CM000668.2:g.136898152T>C	GRCh38
NC_000006.11:g.137219290T>C , CM000668.1:g.137219290T>C	GRCh37
NC_000006.10:g.137260983T>C	NCBI36
NG_008462.1:g.80573T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.814T>C MANE Select	ENSP00000315680.3:p.Phe272Leu
ENST00000541292.6:c.*79T>C	ENSP00000441004.1:n.*79T>C
ENST00000678002.1:c.502T>C
ENST00000678557.1:c.700T>C	ENSP00000502962.1:p.Phe234Leu
ENST00000679286.1:c.694T>C	ENSP00000503168.1:p.Phe232Leu
ENST00000318471.4:c.814T>C	ENSP00000315680.3:p.Phe272Leu
NM_000288.3:c.814T>C	NP_000279.1:p.Phe272Leu
XM_005267019.3:c.700T>C	XP_005267076.1:p.Phe234Leu
XM_006715502.1:c.520T>C	XP_006715565.1:p.Phe174Leu
XM_011535900.1:c.537T>C	XP_011534202.1:p.Thr179=
XM_005267019.4:c.700T>C	XP_005267076.1:p.Phe234Leu
XM_006715502.2:c.520T>C	XP_006715565.1:p.Phe174Leu
XM_017010934.2:c.537T>C	XP_016866423.1:p.Thr179=
NM_000288.4:c.814T>C MANE Select	NP_000279.1:p.Phe272Leu