Canonical Allele Identifier: CA1582937866
Gene: MEIKIN HGNC NCBI

Linked Data

dbSNP Id: rs1355095
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.131913076C>G , CM000667.2:g.131913076C>G GRCh38
NC_000005.9:g.131248769C>G , CM000667.1:g.131248769C>G GRCh37
NC_000005.8:g.131276668C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000442687.6:c.639-1197G>C MANE Select ENSP00000488568.1:n.639-1197G>C
ENST00000652469.1:c.*374-1197G>C ENSP00000498837.1:n.*374-1197G>C
ENST00000413683.5:c.*564-1197G>C ENSP00000415140.1:n.*564-1197G>C
ENST00000442687.5:c.639-1197G>C ENSP00000488568.1:n.639-1197G>C
ENST00000446743.1:n.158-1197G>C
ENST00000616644.2:c.639-1197G>C ENSP00000481155.1:n.639-1197G>C
NM_001303622.1:c.639-1197G>C NP_001290551.1:n.639-1197G>C
NM_001303622.2:c.639-1197G>C MANE Select NP_001290551.1:n.639-1197G>C
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