Canonical Allele Identifier: CA16242325

Gene: MEIKIN

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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