Canonical Allele Identifier: CA12426987

Gene: MLN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33796256C>T , CM000668.2:g.33796256C>T	GRCh38
NC_000006.11:g.33764033C>T , CM000668.1:g.33764033C>T	GRCh37
NC_000006.10:g.33872011C>T	NCBI36
NG_053042.1:g.3019G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430124.7:c.235-651G>A MANE Select	ENSP00000388825.2:n.235-651G>A
ENST00000266003.9:c.235-651G>A	ENSP00000266003.5:n.235-651G>A
ENST00000430124.6:c.235-651G>A	ENSP00000388825.2:n.235-651G>A
ENST00000507738.1:c.235-651G>A	ENSP00000425467.1:n.235-651G>A
NM_001040109.1:c.235-651G>A	NP_001035198.1:n.235-651G>A
NM_001184698.1:c.235-651G>A	NP_001171627.1:n.235-651G>A
NM_002418.2:c.235-651G>A	NP_002409.1:n.235-651G>A
XR_926707.1:n.1443+3101C>T
XR_926708.1:n.227+3101C>T
XR_926709.1:n.1443+3101C>T
XR_001744088.1:n.81+3101C>T
XR_926707.2:n.81+3101C>T
NM_002418.3:c.235-651G>A MANE Select	NP_002409.1:n.235-651G>A
NM_001040109.2:c.235-651G>A	NP_001035198.1:n.235-651G>A
NM_001184698.2:c.235-651G>A	NP_001171627.1:n.235-651G>A