Canonical Allele Identifier: CA1624312901

Gene: PEX6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969864C= , CM000668.2:g.42969864C=	GRCh38
NC_000006.11:g.42937602C= , CM000668.1:g.42937602C=	GRCh37
NC_000006.10:g.43045580C=	NCBI36
NG_008370.1:g.14380G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1233+21G= MANE Select	ENSP00000303511.8:n.1233+21G=
ENST00000244546.4:c.1233+21G=	ENSP00000244546.4:n.1233+21G=
ENST00000304611.12:c.1233+21G=	ENSP00000303511.8:n.1233+21G=
NM_000287.3:c.1233+21G=	NP_000278.3:n.1233+21G=
NM_001316313.1:c.969+21G=	NP_001303242.1:n.969+21G=
NR_133009.1:n.1326+21G=
XM_011514661.1:c.1149+21G=	XP_011512963.1:n.1149+21G=
XR_926246.1:n.1326+21G=
XM_011514661.2:c.1149+21G=	XP_011512963.1:n.1149+21G=
XR_001743466.2:n.2307+21G=
NM_000287.4:c.1233+21G= MANE Select	NP_000278.3:n.1233+21G=
NM_001316313.2:c.969+21G=	NP_001303242.1:n.969+21G=
NR_133009.2:n.1264+21G=