Canonical Allele Identifier: CA8845190
Gene: PYCR1 HGNC NCBI

Linked Data

dbSNP Id: rs765495873

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81932929C>A , CM000679.2:g.81932929C>A GRCh38
NC_000017.10:g.79890805C>A , CM000679.1:g.79890805C>A GRCh37
NC_000017.9:g.77484096C>A NCBI36
NG_023032.1:g.9164G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000329875.13:c.*285G>T MANE Select ENSP00000328858.8:n.*285G>T
ENST00000329875.12:c.*285G>T ENSP00000328858.8:n.*285G>T
ENST00000337943.9:c.902G>T ENSP00000336579.5:p.Gly301Val
ENST00000403172.8:c.*285G>T ENSP00000385483.4:n.*285G>T
ENST00000577756.5:c.*427G>T ENSP00000463352.1:n.*427G>T
ENST00000584848.5:c.949G>T ENSP00000463342.1:n.949G>T
ENST00000619204.4:c.*285G>T ENSP00000479793.1:n.*285G>T
ENST00000629768.2:c.*427G>T ENSP00000485679.1:n.*427G>T
NM_001282279.1:c.*285G>T NP_001269208.1:n.*285G>T
NM_001282280.1:c.*285G>T NP_001269209.1:n.*285G>T
NM_001282281.1:c.*285G>T NP_001269210.1:n.*285G>T
NM_006907.3:c.*285G>T NP_008838.2:n.*285G>T
NM_153824.2:c.902G>T NP_722546.1:p.Gly301Val
XM_005256381.1:c.*285G>T XP_005256438.1:n.*285G>T
XM_011523583.1:c.*285G>T XP_011521885.1:n.*285G>T
XM_011523584.1:c.*285G>T XP_011521886.1:n.*285G>T
XM_011523585.1:c.*427G>T XP_011521887.1:n.*427G>T
NM_001330523.1:c.*427G>T NP_001317452.1:n.*427G>T
XM_005256381.2:c.*285G>T XP_005256438.1:n.*285G>T
XM_011523583.2:c.*285G>T XP_011521885.1:n.*285G>T
XM_011523584.3:c.*285G>T XP_011521886.1:n.*285G>T
XM_011523585.2:c.*427G>T XP_011521887.1:n.*427G>T
XM_024450849.1:c.*285G>T XP_024306617.1:n.*285G>T
NM_001282279.2:c.*285G>T NP_001269208.1:n.*285G>T
NM_001282281.2:c.*285G>T NP_001269210.1:n.*285G>T
NM_006907.4:c.*285G>T MANE Select NP_008838.2:n.*285G>T
NM_153824.3:c.902G>T NP_722546.1:p.Gly301Val
NM_001282280.2:c.*285G>T NP_001269209.1:n.*285G>T
NM_001330523.2:c.*427G>T NP_001317452.1:n.*427G>T