Canonical Allele Identifier: CA222798227

Gene: MS4A15

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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