Canonical Allele Identifier: CA2361537764

Gene: PROCR

Linked Data

• dbSNP Id: rs1600734554

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35175886A>G , CM000682.2:g.35175886A>G	GRCh38
NC_000020.10:g.33763689A>G , CM000682.1:g.33763689A>G	GRCh37
NC_000020.9:g.33227350A>G	NCBI36
NG_032899.1:g.8916A>G
NG_032899.2:g.8916A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-282A>G MANE Select	ENSP00000216968.3:n.323-282A>G
ENST00000216968.4:c.323-282A>G	ENSP00000216968.3:n.323-282A>G
ENST00000635377.1:c.223-282A>G
NM_006404.4:c.323-282A>G	NP_006395.2:n.323-282A>G
XM_011528496.1:c.323-282A>G	XP_011526798.1:n.323-282A>G
NM_001355008.1:c.-101-10015T>C	NP_001341937.1:n.-101-10015T>C
NM_006404.5:c.323-282A>G MANE Select	NP_006395.2:n.323-282A>G
NM_001355008.2:c.-101-10015T>C	NP_001341937.1:n.-101-10015T>C