Canonical Allele Identifier: CA1051820941
Gene: ALCAM HGNC NCBI

Linked Data

dbSNP Id: rs1940967134
gnomAD v3: 3-105576641-A-G
gnomAD v4: 3-105576641-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.105576641A>G , CM000665.2:g.105576641A>G GRCh38
NC_000003.11:g.105295485A>G , CM000665.1:g.105295485A>G GRCh37
NC_000003.10:g.106778175A>G NCBI36
NG_029729.1:g.214929A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000306107.9:c.*2190A>G MANE Select ENSP00000305988.5:n.*2190A>G
ENST00000472644.6:c.*2190A>G ENSP00000419236.2:n.*2190A>G
NM_001243280.1:c.*2190A>G NP_001230209.1:n.*2190A>G
NM_001627.3:c.*2190A>G NP_001618.2:n.*2190A>G
NM_001627.4:c.*2190A>G MANE Select NP_001618.2:n.*2190A>G
NM_001243280.2:c.*2190A>G NP_001230209.1:n.*2190A>G
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