Canonical Allele Identifier: CA1017161505

Gene: PROCR

Linked Data

• dbSNP Id: rs2086010534
• gnomAD v3: 20-35175885-C-CTG
• gnomAD v4: 20-35175885-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175885_35175886insTG , CM000682.2:g.35175885_35175886insTG	GRCh38
NC_000020.10:g.33763688_33763689insTG , CM000682.1:g.33763688_33763689insTG	GRCh37
NC_000020.9:g.33227349_33227350insTG	NCBI36
NG_032899.1:g.8915_8916insTG
NG_032899.2:g.8915_8916insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-283_323-282insTG MANE Select	ENSP00000216968.3:n.323-283_323-282insTG
ENST00000216968.4:c.323-283_323-282insTG	ENSP00000216968.3:n.323-283_323-282insTG
ENST00000635377.1:c.223-283_223-282insTG
NM_006404.4:c.323-283_323-282insTG	NP_006395.2:n.323-283_323-282insTG
XM_011528496.1:c.323-283_323-282insTG	XP_011526798.1:n.323-283_323-282insTG
NM_001355008.1:c.-101-10015_-101-10014insCA	NP_001341937.1:n.-101-10015_-101-10014insCA
NM_006404.5:c.323-283_323-282insTG MANE Select	NP_006395.2:n.323-283_323-282insTG
NM_001355008.2:c.-101-10015_-101-10014insCA	NP_001341937.1:n.-101-10015_-101-10014insCA