Canonical Allele Identifier: CA1283058717
Gene: DBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.119372265A= , CM000664.2:g.119372265A= GRCh38
NC_000002.11:g.120129841A= , CM000664.1:g.120129841A= GRCh37
NC_000002.10:g.119846311A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001079862.4:c.211A= MANE Select NP_001073331.1:p.Met71=
ENST00000355857.8:c.211A= MANE Select ENSP00000348116.3:p.Met71=
NM_001079862.2:c.211A= NP_001073331.1:p.Met71=
NM_001079862.3:c.211A= NP_001073331.1:p.Met71=
NM_001079863.1:c.214A= NP_001073332.1:p.Met72=
NM_001079863.2:c.214A= NP_001073332.1:p.Met72=
NM_001079863.3:c.214A= NP_001073332.1:p.Met72=
NM_001178017.1:c.394A= NP_001171488.1:p.Met132=
NM_001178017.3:c.394A= NP_001171488.1:p.Met132=
NM_001178041.2:c.337A= NP_001171512.1:p.Met113=
NM_001178041.3:c.337A= NP_001171512.1:p.Met113=
NM_001178041.4:c.337A= NP_001171512.1:p.Met113=
NM_001178042.2:c.262A= NP_001171513.1:p.Met88=
NM_001178042.3:c.262A= NP_001171513.1:p.Met88=
NM_001178042.4:c.262A= NP_001171513.1:p.Met88=
NM_001178043.2:c.241A= NP_001171514.1:p.Met81=
NM_001178043.3:c.241A= NP_001171514.1:p.Met81=
NM_001178043.4:c.241A= NP_001171514.1:p.Met81=
NM_001282633.1:c.262A= NP_001269562.1:p.Met88=
NM_001282633.2:c.262A= NP_001269562.1:p.Met88=
NM_001282633.3:c.262A= NP_001269562.1:p.Met88=
NM_001282634.1:c.262A= NP_001269563.1:p.Met88=
NM_001282634.2:c.262A= NP_001269563.1:p.Met88=
NM_001282634.3:c.262A= NP_001269563.1:p.Met88=
NM_001282635.1:c.262A= NP_001269564.1:p.Met88=
NM_001282635.2:c.262A= NP_001269564.1:p.Met88=
NM_001282635.3:c.262A= NP_001269564.1:p.Met88=
NM_001282636.1:c.139A= NP_001269565.1:p.Met47=
NM_001282636.2:c.139A= NP_001269565.1:p.Met47=
NM_001282636.3:c.139A= NP_001269565.1:p.Met47=
NM_001352432.1:c.139A= NP_001339361.1:p.Met47=
NM_001352432.2:c.139A= NP_001339361.1:p.Met47=
NM_001352432.3:c.139A= NP_001339361.1:p.Met47=
NM_020548.7:c.262A= NP_065438.1:p.Met88=
NM_020548.8:c.262A= NP_065438.1:p.Met88=
NM_020548.9:c.262A= NP_065438.1:p.Met88=
NR_104221.1:n.618A=
ENST00000311521.8:c.262A= ENSP00000311117.4:p.Met88=
ENST00000355857.7:c.211A= ENSP00000348116.3:p.Met71=
ENST00000393103.2:c.214A= ENSP00000376815.2:p.Met72=
ENST00000409094.5:c.262A= ENSP00000386486.1:p.Met88=
ENST00000460901.1:n.585A=
ENST00000475783.1:n.607A=
ENST00000535617.5:c.241A= ENSP00000442917.2:p.Met81=
ENST00000535757.5:c.262A= ENSP00000439012.1:p.Met88=
ENST00000542275.5:c.379A= ENSP00000440698.2:p.Met127=
ENST00000627093.2:c.337A= ENSP00000486281.1:p.Met113=
ENST00000627305.2:c.394A= ENSP00000486361.1:p.Met132=