Canonical Allele Identifier: CA2361537765

Gene: PROCR

Linked Data

• dbSNP Id: rs2086010534

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175885_35175886insTGAGCTG , CM000682.2:g.35175885_35175886insTGAGCTG	GRCh38
NC_000020.10:g.33763688_33763689insTGAGCTG , CM000682.1:g.33763688_33763689insTGAGCTG	GRCh37
NC_000020.9:g.33227349_33227350insTGAGCTG	NCBI36
NG_032899.1:g.8915_8916insTGAGCTG
NG_032899.2:g.8915_8916insTGAGCTG

Transcript Alleles

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