Canonical Allele Identifier: CA368204768

Gene: PEX1

Linked Data

• COSMIC: COSM5621488
• MyVariant Identifiers: chr7:g.92151444T>A (hg19) ; chr7:g.92522130T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92522130T>A , CM000669.2:g.92522130T>A	GRCh38
NC_000007.13:g.92151444T>A , CM000669.1:g.92151444T>A	GRCh37
NC_000007.12:g.91989380T>A	NCBI36
NG_008341.1:g.11402A>T
NG_008341.2:g.11402A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.245A>T MANE Select	ENSP00000248633.4:p.Gln82Leu
ENST00000248633.8:c.245A>T	ENSP00000248633.4:p.Gln82Leu
ENST00000428214.5:c.245A>T	ENSP00000394413.1:p.Gln82Leu
ENST00000438045.5:c.245A>T	ENSP00000410438.1:p.Gln82Leu
ENST00000484913.5:n.249A>T
NM_000466.2:c.245A>T	NP_000457.1:p.Gln82Leu
NM_001282677.1:c.245A>T	NP_001269606.1:p.Gln82Leu
NM_001282678.1:c.-415A>T	NP_001269607.1:n.-415A>T
XR_242246.3:n.341A>T
XR_242246.5:n.292A>T
NM_000466.3:c.245A>T MANE Select	NP_000457.1:p.Gln82Leu
NM_001282677.2:c.245A>T	NP_001269606.1:p.Gln82Leu
NM_001282678.2:c.-415A>T	NP_001269607.1:n.-415A>T