Canonical Allele Identifier: CA635336393

Gene: PROCR

Linked Data

• dbSNP Id: rs370936992
• gnomAD v2: 20-33763702-GT-G
• gnomAD v3: 20-35175899-GT-G
• gnomAD v4: 20-35175899-GT-G
• MyVariant Identifiers: chr20:g.33763703del (hg19) ; chr20:g.35175900del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175909del , CM000682.2:g.35175909del	GRCh38
NC_000020.10:g.33763712del , CM000682.1:g.33763712del	GRCh37
NC_000020.9:g.33227373del	NCBI36
NG_032899.1:g.8939del
NG_032899.2:g.8939del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-259del MANE Select	ENSP00000216968.3:n.323-259del
ENST00000216968.4:c.323-259del	ENSP00000216968.3:n.323-259del
ENST00000635377.1:c.223-259del
NM_006404.4:c.323-259del	NP_006395.2:n.323-259del
XM_011528496.1:c.323-259del	XP_011526798.1:n.323-259del
NM_001355008.1:c.-101-10029del	NP_001341937.1:n.-101-10029del
NM_006404.5:c.323-259del MANE Select	NP_006395.2:n.323-259del
NM_001355008.2:c.-101-10029del	NP_001341937.1:n.-101-10029del