Canonical Allele Identifier: CA2683718543
Gene: PEX1 HGNC NCBI

Linked Data

gnomAD v4: 7-92499921-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92499921G>T , CM000669.2:g.92499921G>T GRCh38
NC_000007.13:g.92129235G>T , CM000669.1:g.92129235G>T GRCh37
NC_000007.12:g.91967171G>T NCBI36
NG_008341.1:g.33611C>A
NG_008341.2:g.33611C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2584-83C>A MANE Select ENSP00000248633.4:n.2584-83C>A
ENST00000248633.8:c.2584-83C>A ENSP00000248633.4:n.2584-83C>A
ENST00000428214.5:c.2413-83C>A ENSP00000394413.1:n.2413-83C>A
ENST00000438045.5:c.1618-83C>A ENSP00000410438.1:n.1618-83C>A
ENST00000484913.5:n.2623-83C>A
ENST00000496420.5:n.2476-83C>A
NM_000466.2:c.2584-83C>A NP_000457.1:n.2584-83C>A
NM_001282677.1:c.2413-83C>A NP_001269606.1:n.2413-83C>A
NM_001282678.1:c.1960-83C>A NP_001269607.1:n.1960-83C>A
XM_005250433.3:c.835-83C>A XP_005250490.1:n.835-83C>A
XR_242246.3:n.2680-83C>A
XM_017012319.2:c.835-83C>A XP_016867808.1:n.835-83C>A
XR_001744808.2:n.1611-83C>A
XR_242246.5:n.2631-83C>A
NM_000466.3:c.2584-83C>A MANE Select NP_000457.1:n.2584-83C>A
NM_001282677.2:c.2413-83C>A NP_001269606.1:n.2413-83C>A
NM_001282678.2:c.1960-83C>A NP_001269607.1:n.1960-83C>A