Canonical Allele Identifier: CA381529417
Gene: CABP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67456196A>C , CM000673.2:g.67456196A>C GRCh38
NC_000011.9:g.67223667A>C , CM000673.1:g.67223667A>C GRCh37
NC_000011.8:g.66980243A>C NCBI36
NG_021211.1:g.5850A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325656.7:c.375A>C MANE Select ENSP00000324960.5:p.Glu125Asp
ENST00000325656.6:c.375A>C ENSP00000324960.5:p.Glu125Asp
ENST00000438189.6:c.60A>C ENSP00000401555.2:p.Glu20Asp
ENST00000545777.1:c.*56A>C ENSP00000439145.1:n.*56A>C
NM_001300895.1:c.60A>C NP_001287824.1:p.Glu20Asp
NM_001300896.1:c.60A>C NP_001287825.1:p.Glu20Asp
NM_145200.3:c.375A>C NP_660201.1:p.Glu125Asp
XM_005274114.2:c.435A>C XP_005274171.2:p.Glu145Asp
XM_011545181.1:c.435A>C XP_011543483.1:p.Glu145Asp
XM_011545182.1:c.435A>C XP_011543484.1:p.Glu145Asp
XM_011545183.1:c.60A>C XP_011543485.1:p.Glu20Asp
XM_011545184.1:c.60A>C XP_011543486.1:p.Glu20Asp
XM_005274114.3:c.435A>C XP_005274171.2:p.Glu145Asp
XM_011545181.2:c.435A>C XP_011543483.1:p.Glu145Asp
XM_011545182.2:c.435A>C XP_011543484.1:p.Glu145Asp
XM_011545183.2:c.60A>C XP_011543485.1:p.Glu20Asp
XM_017018025.1:c.60A>C XP_016873514.1:p.Glu20Asp
XM_024448615.1:c.375A>C XP_024304383.1:p.Glu125Asp
XM_024448616.1:c.60A>C XP_024304384.1:p.Glu20Asp
NM_001300895.2:c.60A>C NP_001287824.1:p.Glu20Asp
NM_001300896.2:c.60A>C NP_001287825.1:p.Glu20Asp
NM_145200.4:c.375A>C NP_660201.1:p.Glu125Asp
NM_001300895.3:c.60A>C NP_001287824.1:p.Glu20Asp
NM_001300896.3:c.60A>C NP_001287825.1:p.Glu20Asp
NM_001379183.1:c.60A>C NP_001366112.1:p.Glu20Asp
NM_145200.5:c.375A>C MANE Select NP_660201.1:p.Glu125Asp
NR_166529.1:n.436+407A>C