Canonical Allele Identifier: CA2067518059

Gene: MLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120691123C= , CM000674.2:g.120691123C=	GRCh38
NC_000012.11:g.121128926C= , CM000674.1:g.121128926C=	GRCh37
NC_000012.10:g.119613309C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228506.8:c.236-2968C= MANE Select	ENSP00000228506.3:n.236-2968C=
ENST00000228506.7:c.236-2968C=	ENSP00000228506.3:n.236-2968C=
ENST00000412616.2:c.236-2968C=	ENSP00000440746.1:n.236-2968C=
NM_001303627.1:c.-15+2689C=	NP_001290556.1:n.-15+2689C=
NM_001303628.1:c.236-2968C=	NP_001290557.1:n.236-2968C=
NM_014730.3:c.236-2968C=	NP_055545.1:n.236-2968C=
XM_011539031.1:c.-2020C=	XP_011537333.1:n.-2020C=
XM_011539032.1:c.-1708C=	XP_011537334.1:n.-1708C=
XM_011539033.1:c.-1117C=	XP_011537335.1:n.-1117C=
XM_011539034.1:c.-648+359C=	XP_011537336.1:n.-648+359C=
NM_014730.4:c.236-2968C= MANE Select	NP_055545.1:n.236-2968C=
NM_001303628.2:c.236-2968C=	NP_001290557.1:n.236-2968C=
NM_001303627.2:c.-15+2689C=	NP_001290556.1:n.-15+2689C=