Canonical Allele Identifier: CA2278748898
Gene: PYCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81933270G= , CM000679.2:g.81933270G= GRCh38
NC_000017.10:g.79891146G= , CM000679.1:g.79891146G= GRCh37
NC_000017.9:g.77484437G= NCBI36
NG_023032.1:g.8823C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329875.13:c.904C= MANE Select ENSP00000328858.8:p.Pro302=
ENST00000329875.12:c.904C= ENSP00000328858.8:p.Pro302=
ENST00000337943.9:c.867+37C= ENSP00000336579.5:n.867+37C=
ENST00000402252.6:c.985C= ENSP00000384949.2:p.Pro329=
ENST00000403172.8:c.811C= ENSP00000385483.4:p.Pro271=
ENST00000577756.5:c.*86C= ENSP00000463352.1:n.*86C=
ENST00000584848.5:c.608C= ENSP00000463342.1:n.608C=
ENST00000619204.4:c.904C= ENSP00000479793.1:p.Pro302=
ENST00000629768.2:c.*86C= ENSP00000485679.1:n.*86C=
NM_001282279.1:c.811C= NP_001269208.1:p.Pro271=
NM_001282280.1:c.904C= NP_001269209.1:p.Pro302=
NM_001282281.1:c.985C= NP_001269210.1:p.Pro329=
NM_006907.3:c.904C= NP_008838.2:p.Pro302=
NM_153824.2:c.867+37C= NP_722546.1:n.867+37C=
XM_005256381.1:c.904C= XP_005256438.1:p.Pro302=
XM_011523583.1:c.904C= XP_011521885.1:p.Pro302=
XM_011523584.1:c.904C= XP_011521886.1:p.Pro302=
XM_011523585.1:c.*86C= XP_011521887.1:n.*86C=
NM_001330523.1:c.*86C= NP_001317452.1:n.*86C=
XM_005256381.2:c.904C= XP_005256438.1:p.Pro302=
XM_011523583.2:c.904C= XP_011521885.1:p.Pro302=
XM_011523584.3:c.904C= XP_011521886.1:p.Pro302=
XM_011523585.2:c.*86C= XP_011521887.1:n.*86C=
XM_024450849.1:c.904C= XP_024306617.1:p.Pro302=
NM_001282279.2:c.811C= NP_001269208.1:p.Pro271=
NM_001282281.2:c.985C= NP_001269210.1:p.Pro329=
NM_006907.4:c.904C= MANE Select NP_008838.2:p.Pro302=
NM_153824.3:c.867+37C= NP_722546.1:n.867+37C=
NM_001282280.2:c.904C= NP_001269209.1:p.Pro302=
NM_001330523.2:c.*86C= NP_001317452.1:n.*86C=