Canonical Allele Identifier: CA452374660

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137143824A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136822686A>T , CM000668.2:g.136822686A>T	GRCh38
NC_000006.11:g.137143824A>T , CM000668.1:g.137143824A>T	GRCh37
NC_000006.10:g.137185517A>T	NCBI36
NG_008462.1:g.5107A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.21A>T MANE Select	ENSP00000315680.3:p.Gly7=
ENST00000541292.6:c.21A>T	ENSP00000441004.1:p.Gly7=
ENST00000678593.1:c.21A>T	ENSP00000503841.1:p.Gly7=
ENST00000318471.4:c.21A>T	ENSP00000315680.3:p.Gly7=
ENST00000367756.8:c.21A>T	ENSP00000356730.4:p.Gly7=
ENST00000541292.5:c.21A>T	ENSP00000441004.1:p.Gly7=
NM_000288.3:c.21A>T	NP_000279.1:p.Gly7=
XM_006715502.1:c.21A>T	XP_006715565.1:p.Gly7=
XM_011535900.1:c.21A>T	XP_011534202.1:p.Gly7=
XM_006715502.2:c.21A>T	XP_006715565.1:p.Gly7=
XM_017010934.2:c.21A>T	XP_016866423.1:p.Gly7=
NM_000288.4:c.21A>T MANE Select	NP_000279.1:p.Gly7=