Canonical Allele Identifier: CA1976853053
Gene: MS4A5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.60441258C= , CM000673.2:g.60441258C= GRCh38
NC_000011.9:g.60208731C= , CM000673.1:g.60208731C= GRCh37
NC_000011.8:g.59965307C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000300190.7:c.493-6391C= MANE Select ENSP00000300190.2:n.493-6391C=
ENST00000300190.6:c.493-6391C= ENSP00000300190.2:n.493-6391C=
ENST00000528093.1:c.136-6391C=
ENST00000528905.1:c.260-6391C=
ENST00000531403.5:c.*101-6391C= ENSP00000435192.1:n.*101-6391C=
ENST00000533885.5:c.*103+5743C= ENSP00000435330.1:n.*103+5743C=
NM_023945.2:c.493-6391C= NP_076434.2:n.493-6391C=
NM_023945.3:c.493-6391C= MANE Select NP_076434.2:n.493-6391C=
Search 100 bp 5'
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