Canonical Allele Identifier: CA1017161509

Gene: PROCR

Linked Data

• dbSNP Id: rs2086010641
• gnomAD v3: 20-35175886-A-AGCTGG
• gnomAD v4: 20-35175886-A-AGCTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175888_35175889insTGGGC , CM000682.2:g.35175888_35175889insTGGGC	GRCh38
NC_000020.10:g.33763691_33763692insTGGGC , CM000682.1:g.33763691_33763692insTGGGC	GRCh37
NC_000020.9:g.33227352_33227353insTGGGC	NCBI36
NG_032899.1:g.8918_8919insTGGGC
NG_032899.2:g.8918_8919insTGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-280_323-279insTGGGC MANE Select	ENSP00000216968.3:n.323-280_323-279insTGGGC
ENST00000216968.4:c.323-280_323-279insTGGGC	ENSP00000216968.3:n.323-280_323-279insTGGGC
ENST00000635377.1:c.223-280_223-279insTGGGC
NM_006404.4:c.323-280_323-279insTGGGC	NP_006395.2:n.323-280_323-279insTGGGC
XM_011528496.1:c.323-280_323-279insTGGGC	XP_011526798.1:n.323-280_323-279insTGGGC
NM_001355008.1:c.-101-10016_-101-10015insCCAGC	NP_001341937.1:n.-101-10016_-101-10015insCCAGC
NM_006404.5:c.323-280_323-279insTGGGC MANE Select	NP_006395.2:n.323-280_323-279insTGGGC
NM_001355008.2:c.-101-10016_-101-10015insCCAGC	NP_001341937.1:n.-101-10016_-101-10015insCCAGC