Canonical Allele Identifier: CA2527875484
Gene: ADD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70747779A>G , CM000664.2:g.70747779A>G GRCh38
NC_000002.11:g.70974911A>G , CM000664.1:g.70974911A>G GRCh37
NC_000002.10:g.70828419A>G NCBI36
NG_029481.1:g.25465T>C
NG_029481.2:g.25465T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264436.9:c.-154+20107T>C MANE Select ENSP00000264436.3:n.-154+20107T>C
ENST00000264436.8:c.-154+20107T>C ENSP00000264436.3:n.-154+20107T>C
ENST00000355733.7:c.-154+20107T>C ENSP00000347972.3:n.-154+20107T>C
ENST00000403045.6:c.-154+20107T>C ENSP00000384303.2:n.-154+20107T>C
ENST00000407644.6:c.-154+19825T>C ENSP00000384677.2:n.-154+19825T>C
ENST00000413157.6:c.-154+20107T>C ENSP00000388072.2:n.-154+20107T>C
ENST00000425976.5:c.-154+19551T>C ENSP00000412681.1:n.-154+19551T>C
ENST00000430656.5:c.14+20107T>C ENSP00000398112.1:n.14+20107T>C
ENST00000447731.6:c.-219-6373T>C ENSP00000403722.1:n.-219-6373T>C
ENST00000473232.1:n.315+20107T>C
ENST00000496178.1:n.436+12827T>C
NM_001185054.1:c.-154+19825T>C NP_001171983.1:n.-154+19825T>C
NM_001185055.1:c.14+20107T>C NP_001171984.1:n.14+20107T>C
NM_001617.3:c.-154+20107T>C NP_001608.1:n.-154+20107T>C
NM_017482.3:c.-154+20107T>C NP_059516.2:n.-154+20107T>C
NM_017488.3:c.-154+20107T>C NP_059522.1:n.-154+20107T>C
XM_011532503.1:c.-272+20107T>C XP_011530805.1:n.-272+20107T>C
NM_001617.4:c.-154+20107T>C MANE Select NP_001608.1:n.-154+20107T>C
NM_001185055.2:c.14+20107T>C NP_001171984.1:n.14+20107T>C
NM_017482.4:c.-154+20107T>C NP_059516.2:n.-154+20107T>C
NM_017488.4:c.-154+20107T>C NP_059522.1:n.-154+20107T>C
NM_001185054.2:c.-154+19825T>C NP_001171983.1:n.-154+19825T>C