Canonical Allele Identifier: CA570574019
Gene: PEX7 HGNC NCBI

Linked Data

dbSNP Id: rs1293121096

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136872149A>G , CM000668.2:g.136872149A>G GRCh38
NC_000006.11:g.137193287A>G , CM000668.1:g.137193287A>G GRCh37
NC_000006.10:g.137234980A>G NCBI36
NG_008462.1:g.54570A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318471.5:c.748-49A>G MANE Select ENSP00000315680.3:n.748-49A>G
ENST00000541292.6:c.*13-49A>G ENSP00000441004.1:n.*13-49A>G
ENST00000678002.1:c.436-49A>G
ENST00000678557.1:c.634-49A>G ENSP00000502962.1:n.634-49A>G
ENST00000678593.1:c.753-49A>G ENSP00000503841.1:n.753-49A>G
ENST00000679286.1:c.628-49A>G ENSP00000503168.1:n.628-49A>G
ENST00000318471.4:c.748-49A>G ENSP00000315680.3:n.748-49A>G
NM_000288.3:c.748-49A>G NP_000279.1:n.748-49A>G
XM_005267019.3:c.634-49A>G XP_005267076.1:n.634-49A>G
XM_006715502.1:c.454-49A>G XP_006715565.1:n.454-49A>G
XM_011535900.1:c.526+25968A>G XP_011534202.1:n.526+25968A>G
XM_005267019.4:c.634-49A>G XP_005267076.1:n.634-49A>G
XM_006715502.2:c.454-49A>G XP_006715565.1:n.454-49A>G
XM_017010934.2:c.526+25968A>G XP_016866423.1:n.526+25968A>G
NM_000288.4:c.748-49A>G MANE Select NP_000279.1:n.748-49A>G