Canonical Allele Identifier: CA452227823

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137187820T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866682T>A , CM000668.2:g.136866682T>A	GRCh38
NC_000006.11:g.137187820T>A , CM000668.1:g.137187820T>A	GRCh37
NC_000006.10:g.137229513T>A	NCBI36
NG_008462.1:g.49103T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.582T>A MANE Select	ENSP00000315680.3:p.Ile194=
ENST00000541292.6:c.582T>A	ENSP00000441004.1:p.Ile194=
ENST00000678002.1:c.270T>A
ENST00000678557.1:c.468T>A	ENSP00000502962.1:p.Ile156=
ENST00000678593.1:c.587T>A	ENSP00000503841.1:n.587T>A
ENST00000679286.1:c.462T>A	ENSP00000503168.1:p.Ile154=
ENST00000318471.4:c.582T>A	ENSP00000315680.3:p.Ile194=
ENST00000541292.5:c.582T>A	ENSP00000441004.1:p.Ile194=
NM_000288.3:c.582T>A	NP_000279.1:p.Ile194=
XM_005267019.3:c.468T>A	XP_005267076.1:p.Ile156=
XM_006715502.1:c.340-3208T>A	XP_006715565.1:n.340-3208T>A
XM_011535900.1:c.526+20501T>A	XP_011534202.1:n.526+20501T>A
XM_005267019.4:c.468T>A	XP_005267076.1:p.Ile156=
XM_006715502.2:c.340-3208T>A	XP_006715565.1:n.340-3208T>A
XM_017010934.2:c.526+20501T>A	XP_016866423.1:n.526+20501T>A
NM_000288.4:c.582T>A MANE Select	NP_000279.1:p.Ile194=