Canonical Allele Identifier: CA408710684
Gene: PROCR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176757A>T , CM000682.2:g.35176757A>T GRCh38
NC_000020.10:g.33764560A>T , CM000682.1:g.33764560A>T GRCh37
NC_000020.9:g.33228221A>T NCBI36
NG_032899.1:g.9787A>T
NG_032899.2:g.9787A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000216968.5:c.661A>T MANE Select ENSP00000216968.3:p.Ile221Phe
ENST00000216968.4:c.661A>T ENSP00000216968.3:p.Ile221Phe
ENST00000634509.1:c.94+311A>T ENSP00000489456.1:n.94+311A>T
ENST00000635377.1:c.501+311A>T
NM_006404.4:c.661A>T NP_006395.2:p.Ile221Phe
XM_011528496.1:c.601+311A>T XP_011526798.1:n.601+311A>T
NM_001355008.1:c.-101-10886T>A NP_001341937.1:n.-101-10886T>A
NM_006404.5:c.661A>T MANE Select NP_006395.2:p.Ile221Phe
NM_001355008.2:c.-101-10886T>A NP_001341937.1:n.-101-10886T>A