Canonical Allele Identifier: CA1683032420

Gene: MAD1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2225494C= , CM000669.2:g.2225494C=	GRCh38
NC_000007.13:g.2265129C= , CM000669.1:g.2265129C=	GRCh37
NC_000007.12:g.2231655C=	NCBI36
NG_011518.1:g.12455G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265854.12:c.207G= MANE Select	ENSP00000265854.7:p.Arg69=
ENST00000651235.1:c.*2615G=	ENSP00000498895.1:n.*2615G=
ENST00000265854.11:c.207G=	ENSP00000265854.7:p.Arg69=
ENST00000399654.6:c.207G=	ENSP00000382562.2:p.Arg69=
ENST00000402746.5:c.-124-2740G=	ENSP00000384155.1:n.-124-2740G=
ENST00000406869.5:c.207G=	ENSP00000385334.1:p.Arg69=
ENST00000429625.5:c.-7G=	ENSP00000413139.1:n.-7G=
ENST00000429779.1:c.207G=	ENSP00000395457.1:p.Arg69=
ENST00000455998.5:c.151-2740G=	ENSP00000390099.1:n.151-2740G=
NM_001013836.1:c.207G=	NP_001013858.1:p.Arg69=
NM_001013837.1:c.207G=	NP_001013859.1:p.Arg69=
NM_001304523.1:c.207G=	NP_001291452.1:p.Arg69=
NM_001304524.1:c.-124-2740G=	NP_001291453.1:n.-124-2740G=
NM_003550.2:c.207G=	NP_003541.2:p.Arg69=
XM_005249877.1:c.151-2740G=	XP_005249934.1:n.151-2740G=
XM_011515567.1:c.207G=	XP_011513869.1:p.Arg69=
XM_011515568.1:c.207G=	XP_011513870.1:p.Arg69=
XM_011515570.1:c.207G=	XP_011513872.1:p.Arg69=
XM_011515568.3:c.207G=	XP_011513870.1:p.Arg69=
XM_017012690.1:c.399G=	XP_016868179.1:p.Arg133=
XM_024446951.1:c.207G=	XP_024302719.1:p.Arg69=
XM_024446952.1:c.207G=	XP_024302720.1:p.Arg69=
NM_001013836.2:c.207G= MANE Select	NP_001013858.1:p.Arg69=
NM_001013837.2:c.207G=	NP_001013859.1:p.Arg69=
NM_001304523.2:c.207G=	NP_001291452.1:p.Arg69=
NM_001304524.2:c.-124-2740G=	NP_001291453.1:n.-124-2740G=
NM_003550.3:c.207G=	NP_003541.2:p.Arg69=