Canonical Allele Identifier: CA152540133
Gene: MAD1L1 HGNC NCBI

Linked Data

dbSNP Id: rs11764590
MyVariant Identifiers: chr7:g.1993168C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1993168C>G , CM000669.2:g.1993168C>G GRCh38
NC_000007.13:g.2032803C>G , CM000669.1:g.2032803C>G GRCh37
NC_000007.12:g.1999329C>G NCBI36
NG_011518.1:g.244781G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000265854.12:c.1416+8897G>C MANE Select ENSP00000265854.7:n.1416+8897G>C
ENST00000651235.1:c.*4176+8897G>C ENSP00000498895.1:n.*4176+8897G>C
ENST00000265854.11:c.1416+8897G>C ENSP00000265854.7:n.1416+8897G>C
ENST00000399654.6:c.1416+8897G>C ENSP00000382562.2:n.1416+8897G>C
ENST00000402746.5:c.1140+8897G>C ENSP00000384155.1:n.1140+8897G>C
ENST00000406869.5:c.1416+8897G>C ENSP00000385334.1:n.1416+8897G>C
ENST00000438959.5:c.417+8897G>C ENSP00000414877.1:n.417+8897G>C
ENST00000444373.6:c.186+8897G>C ENSP00000393037.2:n.186+8897G>C
NM_001013836.1:c.1416+8897G>C NP_001013858.1:n.1416+8897G>C
NM_001013837.1:c.1416+8897G>C NP_001013859.1:n.1416+8897G>C
NM_001304523.1:c.1416+8897G>C NP_001291452.1:n.1416+8897G>C
NM_001304524.1:c.1140+8897G>C NP_001291453.1:n.1140+8897G>C
NM_003550.2:c.1416+8897G>C NP_003541.2:n.1416+8897G>C
XM_005249877.1:c.1275+8897G>C XP_005249934.1:n.1275+8897G>C
XM_011515567.1:c.1360-12627G>C XP_011513869.1:n.1360-12627G>C
XM_011515568.1:c.1417-791G>C XP_011513870.1:n.1417-791G>C
XM_011515569.1:c.186+8897G>C XP_011513871.1:n.186+8897G>C
XM_011515571.1:c.186+8897G>C XP_011513873.1:n.186+8897G>C
XM_011515568.3:c.1417-791G>C XP_011513870.1:n.1417-791G>C
XM_011515569.3:c.450+8897G>C XP_011513871.2:n.450+8897G>C
XM_017012690.1:c.1608+8897G>C XP_016868179.1:n.1608+8897G>C
XM_017012691.2:c.186+8897G>C XP_016868180.1:n.186+8897G>C
XM_024446951.1:c.1360-12627G>C XP_024302719.1:n.1360-12627G>C
XM_024446952.1:c.1360-12627G>C XP_024302720.1:n.1360-12627G>C
NM_001013836.2:c.1416+8897G>C MANE Select NP_001013858.1:n.1416+8897G>C
NM_001013837.2:c.1416+8897G>C NP_001013859.1:n.1416+8897G>C
NM_001304523.2:c.1416+8897G>C NP_001291452.1:n.1416+8897G>C
NM_001304524.2:c.1140+8897G>C NP_001291453.1:n.1140+8897G>C
NM_003550.3:c.1416+8897G>C NP_003541.2:n.1416+8897G>C