Canonical Allele Identifier: CA1258761078

Linked Data

dbSNP Id: rs1673372497

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68653185_68653196dup , CM000664.2:g.68653185_68653196dup GRCh38
NC_000002.11:g.68880317_68880328dup , CM000664.1:g.68880317_68880328dup GRCh37
NC_000002.10:g.68733821_68733832dup NCBI36
NG_051312.1:g.14598_14609dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000303786.5:c.486-1695_486-1684dup (PROKR1) MANE Select ENSP00000303775.4:n.486-1695_486-1684dup
ENST00000303786.4:c.486-1695_486-1684dup (PROKR1) ENSP00000303775.3:n.486-1695_486-1684dup
ENST00000394342.2:c.486-1695_486-1684dup (APLF) ENSP00000377874.2:n.486-1695_486-1684dup
ENST00000627740.1:n.1198-1695_1198-1684dup (APLF)
NM_138964.2:c.486-1695_486-1684dup (PROKR1) NP_620414.1:n.486-1695_486-1684dup
NM_138964.3:c.486-1695_486-1684dup (PROKR1) NP_620414.1:n.486-1695_486-1684dup
NM_138964.4:c.486-1695_486-1684dup (PROKR1) MANE Select NP_620414.1:n.486-1695_486-1684dup