Canonical Allele Identifier: CA365763945

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137191037G>A (hg19) ; chr6:g.136869899G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136869899G>A , CM000668.2:g.136869899G>A	GRCh38
NC_000006.11:g.137191037G>A , CM000668.1:g.137191037G>A	GRCh37
NC_000006.10:g.137232730G>A	NCBI36
NG_008462.1:g.52320G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.643G>A MANE Select	ENSP00000315680.3:p.Val215Met
ENST00000541292.6:c.643G>A	ENSP00000441004.1:p.Val215Met
ENST00000678002.1:c.331G>A
ENST00000678557.1:c.529G>A	ENSP00000502962.1:p.Val177Met
ENST00000678593.1:c.648G>A	ENSP00000503841.1:n.648G>A
ENST00000679286.1:c.523G>A	ENSP00000503168.1:p.Val175Met
ENST00000318471.4:c.643G>A	ENSP00000315680.3:p.Val215Met
ENST00000541292.5:c.643G>A	ENSP00000441004.1:p.Val215Met
NM_000288.3:c.643G>A	NP_000279.1:p.Val215Met
XM_005267019.3:c.529G>A	XP_005267076.1:p.Val177Met
XM_006715502.1:c.349G>A	XP_006715565.1:p.Val117Met
XM_011535900.1:c.526+23718G>A	XP_011534202.1:n.526+23718G>A
XM_005267019.4:c.529G>A	XP_005267076.1:p.Val177Met
XM_006715502.2:c.349G>A	XP_006715565.1:p.Val117Met
XM_017010934.2:c.526+23718G>A	XP_016866423.1:n.526+23718G>A
NM_000288.4:c.643G>A MANE Select	NP_000279.1:p.Val215Met