Canonical Allele Identifier: CA368168500

Gene: PEX1 GATAD1

Linked Data

• MyVariant Identifiers: chr7:g.92123851C>A (hg19) ; chr7:g.92494537C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92494537C>A , CM000669.2:g.92494537C>A	GRCh38
NC_000007.13:g.92123851C>A , CM000669.1:g.92123851C>A	GRCh37
NC_000007.12:g.91961787C>A	NCBI36
NG_008341.1:g.38995G>T
NG_008341.2:g.38995G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2876G>T (PEX1) MANE Select	ENSP00000248633.4:p.Arg959Leu
ENST00000248633.8:c.2876G>T (PEX1)	ENSP00000248633.4:p.Arg959Leu
ENST00000428214.5:c.2705G>T (PEX1)	ENSP00000394413.1:p.Arg902Leu
ENST00000438045.5:c.1910G>T (PEX1)	ENSP00000410438.1:p.Arg637Leu
ENST00000484913.5:n.2915G>T (PEX1)
ENST00000496420.5:n.2768G>T (PEX1)
NM_000466.2:c.2876G>T (PEX1)	NP_000457.1:p.Arg959Leu
NM_001282677.1:c.2705G>T (PEX1)	NP_001269606.1:p.Arg902Leu
NM_001282678.1:c.2252G>T (PEX1)	NP_001269607.1:p.Arg751Leu
XM_005250433.3:c.1127G>T (PEX1)	XP_005250490.1:p.Arg376Leu
XR_242246.3:n.2972G>T (PEX1)
XM_017012319.2:c.1127G>T (PEX1)	XP_016867808.1:p.Arg376Leu
XR_001744808.2:n.1903G>T (PEX1)
XR_001744843.2:n.5506C>A (GATAD1)
XR_242246.5:n.2923G>T (PEX1)
XR_927494.3:n.4357C>A (GATAD1)
XR_927503.3:n.4288C>A (GATAD1)
NM_000466.3:c.2876G>T (PEX1) MANE Select	NP_000457.1:p.Arg959Leu
NM_001282677.2:c.2705G>T (PEX1)	NP_001269606.1:p.Arg902Leu
NM_001282678.2:c.2252G>T (PEX1)	NP_001269607.1:p.Arg751Leu