Canonical Allele Identifier: CA50308701

Gene: PROKR1 APLF

Linked Data

• dbSNP Id: rs7577526
• MyVariant Identifiers: chr2:g.68880281A>T (hg19) ; chr2:g.68653149A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.68653149A>T , CM000664.2:g.68653149A>T	GRCh38
NC_000002.11:g.68880281A>T , CM000664.1:g.68880281A>T	GRCh37
NC_000002.10:g.68733785A>T	NCBI36
NG_051312.1:g.14562A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303786.5:c.486-1731A>T (PROKR1) MANE Select	ENSP00000303775.4:n.486-1731A>T
ENST00000303786.4:c.486-1731A>T (PROKR1)	ENSP00000303775.3:n.486-1731A>T
ENST00000394342.2:c.486-1731A>T (APLF)	ENSP00000377874.2:n.486-1731A>T
ENST00000627740.1:n.1198-1731A>T (APLF)
NM_138964.2:c.486-1731A>T (PROKR1)	NP_620414.1:n.486-1731A>T
NM_138964.3:c.486-1731A>T (PROKR1)	NP_620414.1:n.486-1731A>T
NM_138964.4:c.486-1731A>T (PROKR1) MANE Select	NP_620414.1:n.486-1731A>T