Canonical Allele Identifier: CA2838475443

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.922046C>G , CM000669.2:g.922046C>G GRCh38
NC_000007.13:g.961683C>G , CM000669.1:g.961683C>G GRCh37
NC_000007.12:g.928209C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265846.10:c.306-1996G>C (ADAP1) MANE Select ENSP00000265846.5:n.306-1996G>C
ENST00000649206.1:c.306-1996G>C (ADAP1) ENSP00000497220.1:n.306-1996G>C
ENST00000265846.9:c.306-1996G>C (ADAP1) ENSP00000265846.5:n.306-1996G>C
ENST00000435943.1:c.267-1996G>C (ADAP1) ENSP00000394973.1:n.267-1996G>C
ENST00000446141.5:c.254-1996G>C (ADAP1)
ENST00000449296.6:c.90-1996G>C (ADAP1) ENSP00000407267.2:n.90-1996G>C
ENST00000453823.5:c.134-1996G>C (ADAP1)
ENST00000454383.5:c.127-1996G>C (ADAP1)
ENST00000457254.5:c.*49-1996G>C (COX19) ENSP00000413423.1:n.*49-1996G>C
ENST00000463358.5:n.279-1996G>C (ADAP1)
ENST00000477906.5:n.298-1996G>C (ADAP1)
ENST00000488527.5:n.362+931G>C (ADAP1)
ENST00000495686.1:n.504-1996G>C (ADAP1)
ENST00000539900.5:c.339-1996G>C (ADAP1) ENSP00000442682.1:n.339-1996G>C
ENST00000611167.4:c.90-1996G>C (ADAP1) ENSP00000481154.1:n.90-1996G>C
NM_001284308.1:c.339-1996G>C (ADAP1) NP_001271237.1:n.339-1996G>C
NM_001284309.1:c.90-1996G>C (ADAP1) NP_001271238.1:n.90-1996G>C
NM_001284310.1:c.90-1996G>C (ADAP1) NP_001271239.1:n.90-1996G>C
NM_006869.3:c.306-1996G>C (ADAP1) NP_006860.1:n.306-1996G>C
NM_006869.4:c.306-1996G>C (ADAP1) MANE Select NP_006860.2:n.306-1996G>C
NM_001284309.2:c.90-1996G>C (ADAP1) NP_001271238.2:n.90-1996G>C
NM_001284308.2:c.339-1996G>C (ADAP1) NP_001271237.2:n.339-1996G>C
NM_001284310.2:c.90-1996G>C (ADAP1) NP_001271239.2:n.90-1996G>C