Canonical Allele Identifier: CA313480749

Gene: PROCR

Linked Data

• dbSNP Id: rs916539626
• gnomAD v2: 20-33763699-CCT-C
• gnomAD v3: 20-35175896-CCT-C
• gnomAD v4: 20-35175896-CCT-C
• MyVariant Identifiers: chr20:g.33763700_33763701del (hg19) ; chr20:g.35175897_35175898del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175897_35175898del , CM000682.2:g.35175897_35175898del	GRCh38
NC_000020.10:g.33763700_33763701del , CM000682.1:g.33763700_33763701del	GRCh37
NC_000020.9:g.33227361_33227362del	NCBI36
NG_032899.1:g.8927_8928del
NG_032899.2:g.8927_8928del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-271_323-270del MANE Select	ENSP00000216968.3:n.323-271_323-270del
ENST00000216968.4:c.323-271_323-270del	ENSP00000216968.3:n.323-271_323-270del
ENST00000635377.1:c.223-271_223-270del
NM_006404.4:c.323-271_323-270del	NP_006395.2:n.323-271_323-270del
XM_011528496.1:c.323-271_323-270del	XP_011526798.1:n.323-271_323-270del
NM_001355008.1:c.-101-10027_-101-10026del	NP_001341937.1:n.-101-10027_-101-10026del
NM_006404.5:c.323-271_323-270del MANE Select	NP_006395.2:n.323-271_323-270del
NM_001355008.2:c.-101-10027_-101-10026del	NP_001341937.1:n.-101-10027_-101-10026del