Canonical Allele Identifier: CA646013201

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186453392A>T , CM000663.2:g.186453392A>T GRCh38
NC_000001.10:g.186422524A>T , CM000663.1:g.186422524A>T GRCh37
NC_000001.9:g.184689147A>T NCBI36
NG_009101.1:g.12716T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000391997.3:c.-24-3909T>A (PDC) MANE Select ENSP00000375855.2:n.-24-3909T>A
ENST00000391997.2:c.-24-3909T>A (PDC) ENSP00000375855.2:n.-24-3909T>A
NM_002597.4:c.-24-3909T>A (PDC) NP_002588.3:n.-24-3909T>A
NR_126002.1:n.441+2118A>T (PDC-AS1)
NM_002597.5:c.-24-3909T>A (PDC) MANE Select NP_002588.3:n.-24-3909T>A