Canonical Allele Identifier: CA2652596903

Gene: PROCR

Linked Data

• gnomAD v4: 20-35176768-TGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176770_35176772del , CM000682.2:g.35176770_35176772del	GRCh38
NC_000020.10:g.33764573_33764575del , CM000682.1:g.33764573_33764575del	GRCh37
NC_000020.9:g.33228234_33228236del	NCBI36
NG_032899.1:g.9800_9802del
NG_032899.2:g.9800_9802del

Transcript Alleles

HGVS	Amino-acid change
ENST00000216968.5:c.674_676del MANE Select	ENSP00000216968.3:p.Val225del
ENST00000216968.4:c.674_676del	ENSP00000216968.3:p.Val225del
ENST00000634509.1:c.94+324_94+326del	ENSP00000489456.1:n.94+324_94+326del
ENST00000635377.1:c.502-317_502-315del
NM_006404.4:c.674_676del	NP_006395.2:p.Val225del
XM_011528496.1:c.601+324_601+326del	XP_011526798.1:n.601+324_601+326del
NM_001355008.1:c.-101-10900_-101-10898del	NP_001341937.1:n.-101-10900_-101-10898del
NM_006404.5:c.674_676del MANE Select	NP_006395.2:p.Val225del
NM_001355008.2:c.-101-10900_-101-10898del	NP_001341937.1:n.-101-10900_-101-10898del