Canonical Allele Identifier: CA1258761272
Gene: PROKR1 HGNC NCBI
APLF HGNC NCBI

Linked Data

dbSNP Id: rs1391965469
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68653424_68653425insA , CM000664.2:g.68653424_68653425insA GRCh38
NC_000002.11:g.68880556_68880557insA , CM000664.1:g.68880556_68880557insA GRCh37
NC_000002.10:g.68734060_68734061insA NCBI36
NG_051312.1:g.14837_14838insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000303786.5:c.486-1456_486-1455insA (PROKR1) MANE Select ENSP00000303775.4:n.486-1456_486-1455insA
ENST00000303786.4:c.486-1456_486-1455insA (PROKR1) ENSP00000303775.3:n.486-1456_486-1455insA
ENST00000394342.2:c.486-1456_486-1455insA (APLF) ENSP00000377874.2:n.486-1456_486-1455insA
ENST00000627740.1:n.1198-1456_1198-1455insA (APLF)
NM_138964.2:c.486-1456_486-1455insA (PROKR1) NP_620414.1:n.486-1456_486-1455insA
NM_138964.3:c.486-1456_486-1455insA (PROKR1) NP_620414.1:n.486-1456_486-1455insA
NM_138964.4:c.486-1456_486-1455insA (PROKR1) MANE Select NP_620414.1:n.486-1456_486-1455insA
Search 100 bp 5'
Search 100 bp 3'