Canonical Allele Identifier: CA2773216358

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136898382_136898387del , CM000668.2:g.136898382_136898387del	GRCh38
NC_000006.11:g.137219520_137219525del , CM000668.1:g.137219520_137219525del	GRCh37
NC_000006.10:g.137261213_137261218del	NCBI36
NG_008462.1:g.80803_80808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.903+141_903+146del MANE Select	ENSP00000315680.3:n.903+141_903+146del
ENST00000541292.6:c.*168+141_*168+146del	ENSP00000441004.1:n.*168+141_*168+146del
ENST00000678002.1:c.591+141_591+146del
ENST00000678557.1:c.789+141_789+146del	ENSP00000502962.1:n.789+141_789+146del
ENST00000679286.1:c.783+141_783+146del	ENSP00000503168.1:n.783+141_783+146del
ENST00000318471.4:c.903+141_903+146del	ENSP00000315680.3:n.903+141_903+146del
NM_000288.3:c.903+141_903+146del	NP_000279.1:n.903+141_903+146del
XM_005267019.3:c.789+141_789+146del	XP_005267076.1:n.789+141_789+146del
XM_006715502.1:c.609+141_609+146del	XP_006715565.1:n.609+141_609+146del
XM_005267019.4:c.789+141_789+146del	XP_005267076.1:n.789+141_789+146del
XM_006715502.2:c.609+141_609+146del	XP_006715565.1:n.609+141_609+146del
XM_017010934.2:c.*26+141_*26+146del	XP_016866423.1:n.*26+141_*26+146del
NM_000288.4:c.903+141_903+146del MANE Select	NP_000279.1:n.903+141_903+146del