Canonical Allele Identifier: CA2278748719

Gene: PYCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81932932T= , CM000679.2:g.81932932T=	GRCh38
NC_000017.10:g.79890808T= , CM000679.1:g.79890808T=	GRCh37
NC_000017.9:g.77484099T=	NCBI36
NG_023032.1:g.9161A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329875.13:c.*282A= MANE Select	ENSP00000328858.8:n.*282A=
ENST00000329875.12:c.*282A=	ENSP00000328858.8:n.*282A=
ENST00000337943.9:c.899A=	ENSP00000336579.5:p.Glu300=
ENST00000403172.8:c.*282A=	ENSP00000385483.4:n.*282A=
ENST00000577756.5:c.*424A=	ENSP00000463352.1:n.*424A=
ENST00000584848.5:c.946A=	ENSP00000463342.1:n.946A=
ENST00000619204.4:c.*282A=	ENSP00000479793.1:n.*282A=
ENST00000629768.2:c.*424A=	ENSP00000485679.1:n.*424A=
NM_001282279.1:c.*282A=	NP_001269208.1:n.*282A=
NM_001282280.1:c.*282A=	NP_001269209.1:n.*282A=
NM_001282281.1:c.*282A=	NP_001269210.1:n.*282A=
NM_006907.3:c.*282A=	NP_008838.2:n.*282A=
NM_153824.2:c.899A=	NP_722546.1:p.Glu300=
XM_005256381.1:c.*282A=	XP_005256438.1:n.*282A=
XM_011523583.1:c.*282A=	XP_011521885.1:n.*282A=
XM_011523584.1:c.*282A=	XP_011521886.1:n.*282A=
XM_011523585.1:c.*424A=	XP_011521887.1:n.*424A=
NM_001330523.1:c.*424A=	NP_001317452.1:n.*424A=
XM_005256381.2:c.*282A=	XP_005256438.1:n.*282A=
XM_011523583.2:c.*282A=	XP_011521885.1:n.*282A=
XM_011523584.3:c.*282A=	XP_011521886.1:n.*282A=
XM_011523585.2:c.*424A=	XP_011521887.1:n.*424A=
XM_024450849.1:c.*282A=	XP_024306617.1:n.*282A=
NM_001282279.2:c.*282A=	NP_001269208.1:n.*282A=
NM_001282281.2:c.*282A=	NP_001269210.1:n.*282A=
NM_006907.4:c.*282A= MANE Select	NP_008838.2:n.*282A=
NM_153824.3:c.899A=	NP_722546.1:p.Glu300=
NM_001282280.2:c.*282A=	NP_001269209.1:n.*282A=
NM_001330523.2:c.*424A=	NP_001317452.1:n.*424A=