Canonical Allele Identifier: CA365764136

Gene: PEX7

Linked Data

• MyVariant Identifiers: chr6:g.137191129T>G (hg19) ; chr6:g.136869991T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136869991T>G , CM000668.2:g.136869991T>G	GRCh38
NC_000006.11:g.137191129T>G , CM000668.1:g.137191129T>G	GRCh37
NC_000006.10:g.137232822T>G	NCBI36
NG_008462.1:g.52412T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000318471.5:c.735T>G MANE Select	ENSP00000315680.3:p.Ile245Met
ENST00000541292.6:c.735T>G	ENSP00000441004.1:p.Ile245Met
ENST00000678002.1:c.423T>G
ENST00000678557.1:c.621T>G	ENSP00000502962.1:p.Ile207Met
ENST00000678593.1:c.740T>G	ENSP00000503841.1:n.740T>G
ENST00000679286.1:c.615T>G	ENSP00000503168.1:p.Ile205Met
ENST00000318471.4:c.735T>G	ENSP00000315680.3:p.Ile245Met
ENST00000541292.5:c.735T>G	ENSP00000441004.1:p.Ile245Met
NM_000288.3:c.735T>G	NP_000279.1:p.Ile245Met
XM_005267019.3:c.621T>G	XP_005267076.1:p.Ile207Met
XM_006715502.1:c.441T>G	XP_006715565.1:p.Ile147Met
XM_011535900.1:c.526+23810T>G	XP_011534202.1:n.526+23810T>G
XM_005267019.4:c.621T>G	XP_005267076.1:p.Ile207Met
XM_006715502.2:c.441T>G	XP_006715565.1:p.Ile147Met
XM_017010934.2:c.526+23810T>G	XP_016866423.1:n.526+23810T>G
NM_000288.4:c.735T>G MANE Select	NP_000279.1:p.Ile245Met