Canonical Allele Identifier: CA1682873660

Gene: MAD1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1977759G= , CM000669.2:g.1977759G=	GRCh38
NC_000007.13:g.2017394G= , CM000669.1:g.2017394G=	GRCh37
NC_000007.12:g.1983920G=	NCBI36
NG_011518.1:g.260190C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265854.12:c.1505+2694C= MANE Select	ENSP00000265854.7:n.1505+2694C=
ENST00000651235.1:c.*4265+2694C=	ENSP00000498895.1:n.*4265+2694C=
ENST00000265854.11:c.1505+2694C=	ENSP00000265854.7:n.1505+2694C=
ENST00000399654.6:c.1505+2694C=	ENSP00000382562.2:n.1505+2694C=
ENST00000402746.5:c.1229+2694C=	ENSP00000384155.1:n.1229+2694C=
ENST00000406869.5:c.1505+2694C=	ENSP00000385334.1:n.1505+2694C=
ENST00000438959.5:c.506+2694C=	ENSP00000414877.1:n.506+2694C=
ENST00000450235.5:c.158+2694C=	ENSP00000394886.1:n.158+2694C=
NM_001013836.1:c.1505+2694C=	NP_001013858.1:n.1505+2694C=
NM_001013837.1:c.1505+2694C=	NP_001013859.1:n.1505+2694C=
NM_001304523.1:c.1505+2694C=	NP_001291452.1:n.1505+2694C=
NM_001304524.1:c.1229+2694C=	NP_001291453.1:n.1229+2694C=
NM_003550.2:c.1505+2694C=	NP_003541.2:n.1505+2694C=
XM_005249877.1:c.1364+2694C=	XP_005249934.1:n.1364+2694C=
XM_011515567.1:c.1448+2694C=	XP_011513869.1:n.1448+2694C=
XM_011515569.1:c.275+2694C=	XP_011513871.1:n.275+2694C=
XM_011515571.1:c.275+2694C=	XP_011513873.1:n.275+2694C=
XM_011515569.3:c.539+2694C=	XP_011513871.2:n.539+2694C=
XM_017012690.1:c.1697+2694C=	XP_016868179.1:n.1697+2694C=
XM_017012691.2:c.275+2694C=	XP_016868180.1:n.275+2694C=
XM_024446951.1:c.1448+2694C=	XP_024302719.1:n.1448+2694C=
XM_024446952.1:c.1448+2694C=	XP_024302720.1:n.1448+2694C=
NM_001013836.2:c.1505+2694C= MANE Select	NP_001013858.1:n.1505+2694C=
NM_001013837.2:c.1505+2694C=	NP_001013859.1:n.1505+2694C=
NM_001304523.2:c.1505+2694C=	NP_001291452.1:n.1505+2694C=
NM_001304524.2:c.1229+2694C=	NP_001291453.1:n.1229+2694C=
NM_003550.3:c.1505+2694C=	NP_003541.2:n.1505+2694C=