Canonical Allele Identifier: CA1390727998
Gene: ALCAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.105576519C= , CM000665.2:g.105576519C= GRCh38
NC_000003.11:g.105295363C= , CM000665.1:g.105295363C= GRCh37
NC_000003.10:g.106778053C= NCBI36
NG_029729.1:g.214807C=

Transcript Alleles

HGVS Amino-acid change
ENST00000306107.9:c.*2068C= MANE Select ENSP00000305988.5:n.*2068C=
ENST00000472644.6:c.*2068C= ENSP00000419236.2:n.*2068C=
NM_001243280.1:c.*2068C= NP_001230209.1:n.*2068C=
NM_001627.3:c.*2068C= NP_001618.2:n.*2068C=
NM_001627.4:c.*2068C= MANE Select NP_001618.2:n.*2068C=
NM_001243280.2:c.*2068C= NP_001230209.1:n.*2068C=
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