Canonical Allele Identifier: CA2580072744
Community Standard Title: NM_001745.4(CAMLG):c.633+4A>G
Gene: CAMLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134741527A>G , CM000667.2:g.134741527A>G GRCh38
NC_000005.9:g.134077217A>G , CM000667.1:g.134077217A>G GRCh37
NC_000005.8:g.134105116A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001745.4:c.633+4A>G MANE Select NP_001736.1:n.633+4A>G
ENST00000297156.4:c.633+4A>G MANE Select ENSP00000297156.2:n.633+4A>G
NM_001745.3:c.633+4A>G NP_001736.1:n.633+4A>G
ENST00000297156.3:c.633+4A>G ENSP00000297156.2:n.633+4A>G
ENST00000514518.1:c.173-2460A>G ENSP00000427331.1:n.173-2460A>G
ENST00000676819.1:n.3027+4A>G
ENST00000676829.1:c.172+2735A>G ENSP00000503328.1:n.172+2735A>G
ENST00000677273.1:c.633+4A>G ENSP00000503312.1:n.633+4A>G
ENST00000677966.1:n.1784A>G
ENST00000678434.1:n.745A>G
ENST00000678771.1:c.630+4A>G ENSP00000504018.1:n.630+4A>G
XM_011543653.1:c.633+4A>G XP_011541955.1:n.633+4A>G