Canonical Allele Identifier: CA1652948659

Gene: PREP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.105394455T= , CM000668.2:g.105394455T=	GRCh38
NC_000006.11:g.105842330T= , CM000668.1:g.105842330T=	GRCh37
NC_000006.10:g.105949023T=	NCBI36
NG_011472.1:g.13640A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369110.8:c.-79+3398A=	ENSP00000358106.4:n.-79+3398A=
ENST00000652536.2:c.120+3398A= MANE Select	ENSP00000499089.1:n.120+3398A=
ENST00000369110.7:c.120+3398A=	ENSP00000358106.3:n.120+3398A=
NM_002726.4:c.120+3398A=	NP_002717.3:n.120+3398A=
XM_005267044.1:c.120+3398A=	XP_005267101.1:n.120+3398A=
XM_011535925.1:c.120+3398A=	XP_011534227.1:n.120+3398A=
XM_005267044.3:c.120+3398A=	XP_005267101.1:n.120+3398A=
XM_011535925.3:c.120+3398A=	XP_011534227.1:n.120+3398A=
NM_002726.5:c.120+3398A= MANE Select	NP_002717.3:n.120+3398A=