Canonical Allele Identifier: CA1977010284
Gene: MS4A15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.60758313A>T , CM000673.2:g.60758313A>T GRCh38
NC_000011.9:g.60525786A>T , CM000673.1:g.60525786A>T GRCh37
NC_000011.8:g.60282362A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405633.4:c.-29+1255A>T MANE Select ENSP00000386022.3:n.-29+1255A>T
ENST00000337911.8:c.-21+1255A>T ENSP00000338692.4:n.-21+1255A>T
ENST00000405633.3:c.-29+1255A>T ENSP00000386022.3:n.-29+1255A>T
ENST00000429322.6:c.-29+1255A>T ENSP00000413918.2:n.-29+1255A>T
ENST00000528170.5:c.-29+1255A>T ENSP00000434165.1:n.-29+1255A>T
NM_001098835.1:c.-29+1255A>T NP_001092305.1:n.-29+1255A>T
NM_001278242.1:c.-29+1255A>T NP_001265171.1:n.-29+1255A>T
NM_152717.2:c.-21+1255A>T NP_689930.1:n.-21+1255A>T
NR_103481.1:n.192+1255A>T
XM_006718458.2:c.-29+1255A>T XP_006718521.1:n.-29+1255A>T
XM_006718459.2:c.-55+1255A>T XP_006718522.1:n.-55+1255A>T
XM_011544812.1:c.-15+1255A>T XP_011543114.1:n.-15+1255A>T
XM_011544814.1:c.-274+1255A>T XP_011543116.1:n.-274+1255A>T
XM_006718459.4:c.-55+1255A>T XP_006718522.1:n.-55+1255A>T
XM_011544812.3:c.-15+1255A>T XP_011543114.1:n.-15+1255A>T
NM_001098835.2:c.-29+1255A>T MANE Select NP_001092305.1:n.-29+1255A>T
NM_001278242.2:c.-29+1255A>T NP_001265171.1:n.-29+1255A>T
NM_152717.3:c.-21+1255A>T NP_689930.1:n.-21+1255A>T
NR_103481.2:n.192+1255A>T