Canonical Allele Identifier: CA1390728002
Gene: ALCAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.105576534A= , CM000665.2:g.105576534A= GRCh38
NC_000003.11:g.105295378A= , CM000665.1:g.105295378A= GRCh37
NC_000003.10:g.106778068A= NCBI36
NG_029729.1:g.214822A=

Transcript Alleles

HGVS Amino-acid change
ENST00000306107.9:c.*2083A= MANE Select ENSP00000305988.5:n.*2083A=
ENST00000472644.6:c.*2083A= ENSP00000419236.2:n.*2083A=
NM_001243280.1:c.*2083A= NP_001230209.1:n.*2083A=
NM_001627.3:c.*2083A= NP_001618.2:n.*2083A=
NM_001627.4:c.*2083A= MANE Select NP_001618.2:n.*2083A=
NM_001243280.2:c.*2083A= NP_001230209.1:n.*2083A=