Canonical Allele Identifier: CA1017161619

Gene: PROCR

Linked Data

• dbSNP Id: rs2086012892
• gnomAD v3: 20-35176071-ACT-A
• gnomAD v4: 20-35176071-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176074_35176075del , CM000682.2:g.35176074_35176075del	GRCh38
NC_000020.10:g.33763877_33763878del , CM000682.1:g.33763877_33763878del	GRCh37
NC_000020.9:g.33227538_33227539del	NCBI36
NG_032899.1:g.9104_9105del
NG_032899.2:g.9104_9105del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-94_323-93del MANE Select	ENSP00000216968.3:n.323-94_323-93del
ENST00000216968.4:c.323-94_323-93del	ENSP00000216968.3:n.323-94_323-93del
ENST00000635377.1:c.223-94_223-93del
NM_006404.4:c.323-94_323-93del	NP_006395.2:n.323-94_323-93del
XM_011528496.1:c.323-94_323-93del	XP_011526798.1:n.323-94_323-93del
NM_001355008.1:c.-101-10202_-101-10201del	NP_001341937.1:n.-101-10202_-101-10201del
NM_006404.5:c.323-94_323-93del MANE Select	NP_006395.2:n.323-94_323-93del
NM_001355008.2:c.-101-10202_-101-10201del	NP_001341937.1:n.-101-10202_-101-10201del