Canonical Allele Identifier: CA2361537776

Gene: PROCR

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175899_35175900delinsGT , CM000682.2:g.35175899_35175900delinsGT	GRCh38
NC_000020.10:g.33763702_33763703delinsGT , CM000682.1:g.33763702_33763703delinsGT	GRCh37
NC_000020.9:g.33227363_33227364delinsGT	NCBI36
NG_032899.1:g.8929_8930delinsGT
NG_032899.2:g.8929_8930delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-269_323-268delinsGT MANE Select	ENSP00000216968.3:n.323-269_323-268delinsGT
ENST00000216968.4:c.323-269_323-268delinsGT	ENSP00000216968.3:n.323-269_323-268delinsGT
ENST00000635377.1:c.223-269_223-268delinsGT
NM_006404.4:c.323-269_323-268delinsGT	NP_006395.2:n.323-269_323-268delinsGT
XM_011528496.1:c.323-269_323-268delinsGT	XP_011526798.1:n.323-269_323-268delinsGT
NM_001355008.1:c.-101-10029_-101-10028delinsAC	NP_001341937.1:n.-101-10029_-101-10028delinsAC
NM_006404.5:c.323-269_323-268delinsGT MANE Select	NP_006395.2:n.323-269_323-268delinsGT
NM_001355008.2:c.-101-10029_-101-10028delinsAC	NP_001341937.1:n.-101-10029_-101-10028delinsAC