Canonical Allele Identifier: CA1017161575

Gene: PROCR

Linked Data

• dbSNP Id: rs2086011607
• gnomAD v3: 20-35175962-GC-G
• gnomAD v4: 20-35175962-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175966del , CM000682.2:g.35175966del	GRCh38
NC_000020.10:g.33763769del , CM000682.1:g.33763769del	GRCh37
NC_000020.9:g.33227430del	NCBI36
NG_032899.1:g.8996del
NG_032899.2:g.8996del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-202del MANE Select	ENSP00000216968.3:n.323-202del
ENST00000216968.4:c.323-202del	ENSP00000216968.3:n.323-202del
ENST00000635377.1:c.223-202del
NM_006404.4:c.323-202del	NP_006395.2:n.323-202del
XM_011528496.1:c.323-202del	XP_011526798.1:n.323-202del
NM_001355008.1:c.-101-10092del	NP_001341937.1:n.-101-10092del
NM_006404.5:c.323-202del MANE Select	NP_006395.2:n.323-202del
NM_001355008.2:c.-101-10092del	NP_001341937.1:n.-101-10092del