Canonical Allele Identifier: CA365766729

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137219341A>T (hg19) ; chr6:g.136898203A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898203A>T , CM000668.2:g.136898203A>T	GRCh38
NC_000006.11:g.137219341A>T , CM000668.1:g.137219341A>T	GRCh37
NC_000006.10:g.137261034A>T	NCBI36
NG_008462.1:g.80624A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.865A>T MANE Select	ENSP00000315680.3:p.Thr289Ser
ENST00000541292.6:c.*130A>T	ENSP00000441004.1:n.*130A>T
ENST00000678002.1:c.553A>T
ENST00000678557.1:c.751A>T	ENSP00000502962.1:p.Thr251Ser
ENST00000679286.1:c.745A>T	ENSP00000503168.1:p.Thr249Ser
ENST00000318471.4:c.865A>T	ENSP00000315680.3:p.Thr289Ser
NM_000288.3:c.865A>T	NP_000279.1:p.Thr289Ser
XM_005267019.3:c.751A>T	XP_005267076.1:p.Thr251Ser
XM_006715502.1:c.571A>T	XP_006715565.1:p.Thr191Ser
XM_011535900.1:c.588A>T	XP_011534202.1:p.Leu196Phe
XM_005267019.4:c.751A>T	XP_005267076.1:p.Thr251Ser
XM_006715502.2:c.571A>T	XP_006715565.1:p.Thr191Ser
XM_017010934.2:c.588A>T	XP_016866423.1:p.Leu196Phe
NM_000288.4:c.865A>T MANE Select	NP_000279.1:p.Thr289Ser