Canonical Allele Identifier: CA1258761028

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68653100_68653102delinsTTG , CM000664.2:g.68653100_68653102delinsTTG GRCh38
NC_000002.11:g.68880232_68880234delinsTTG , CM000664.1:g.68880232_68880234delinsTTG GRCh37
NC_000002.10:g.68733736_68733738delinsTTG NCBI36
NG_051312.1:g.14513_14515delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000303786.5:c.486-1780_486-1778delinsTTG (PROKR1) MANE Select ENSP00000303775.4:n.486-1780_486-1778delinsTTG
ENST00000303786.4:c.486-1780_486-1778delinsTTG (PROKR1) ENSP00000303775.3:n.486-1780_486-1778delinsTTG
ENST00000394342.2:c.486-1780_486-1778delinsTTG (APLF) ENSP00000377874.2:n.486-1780_486-1778delinsTTG
ENST00000627740.1:n.1198-1780_1198-1778delinsTTG (APLF)
NM_138964.2:c.486-1780_486-1778delinsTTG (PROKR1) NP_620414.1:n.486-1780_486-1778delinsTTG
NM_138964.3:c.486-1780_486-1778delinsTTG (PROKR1) NP_620414.1:n.486-1780_486-1778delinsTTG
NM_138964.4:c.486-1780_486-1778delinsTTG (PROKR1) MANE Select NP_620414.1:n.486-1780_486-1778delinsTTG