Canonical Allele Identifier: CA2361537814

Gene: PROCR

Linked Data

• dbSNP Id: rs2086011709

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175969_35175971del , CM000682.2:g.35175969_35175971del	GRCh38
NC_000020.10:g.33763772_33763774del , CM000682.1:g.33763772_33763774del	GRCh37
NC_000020.9:g.33227433_33227435del	NCBI36
NG_032899.1:g.8999_9001del
NG_032899.2:g.8999_9001del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-199_323-197del MANE Select	ENSP00000216968.3:n.323-199_323-197del
ENST00000216968.4:c.323-199_323-197del	ENSP00000216968.3:n.323-199_323-197del
ENST00000635377.1:c.223-199_223-197del
NM_006404.4:c.323-199_323-197del	NP_006395.2:n.323-199_323-197del
XM_011528496.1:c.323-199_323-197del	XP_011526798.1:n.323-199_323-197del
NM_001355008.1:c.-101-10097_-101-10095del	NP_001341937.1:n.-101-10097_-101-10095del
NM_006404.5:c.323-199_323-197del MANE Select	NP_006395.2:n.323-199_323-197del
NM_001355008.2:c.-101-10097_-101-10095del	NP_001341937.1:n.-101-10097_-101-10095del