Canonical Allele Identifier: CA1153748281
Gene: MAD2L2 HGNC NCBI

Linked Data

dbSNP Id: rs1640771288

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11676473A>C , CM000663.2:g.11676473A>C GRCh38
NC_000001.10:g.11736530A>C , CM000663.1:g.11736530A>C GRCh37
NC_000001.9:g.11659117A>C NCBI36
NG_052907.1:g.20316T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376664.11:n.448-333T>G
ENST00000456915.2:c.333-333T>G ENSP00000400982.2:n.333-333T>G
ENST00000697273.1:c.*152-333T>G ENSP00000513220.1:n.*152-333T>G
ENST00000697274.1:c.333-333T>G ENSP00000513221.1:n.333-333T>G
ENST00000376692.9:c.333-333T>G MANE Select ENSP00000365882.4:n.333-333T>G
ENST00000235310.7:c.333-333T>G ENSP00000235310.2:n.333-333T>G
ENST00000376664.10:n.418-333T>G
ENST00000376667.7:c.333-333T>G ENSP00000365855.3:n.333-333T>G
ENST00000376669.9:c.372-333T>G ENSP00000365857.5:n.372-333T>G
ENST00000376672.5:c.372-333T>G ENSP00000365860.1:n.372-333T>G
ENST00000376692.8:c.333-333T>G ENSP00000365882.4:n.333-333T>G
ENST00000445656.5:c.423-333T>G ENSP00000411807.1:n.423-333T>G
ENST00000456915.1:c.333-333T>G ENSP00000400982.1:n.333-333T>G
NM_001127325.1:c.333-333T>G NP_001120797.1:n.333-333T>G
NM_006341.3:c.333-333T>G NP_006332.3:n.333-333T>G
XM_011540507.1:c.333-333T>G XP_011538809.1:n.333-333T>G
XM_024450407.1:c.423-333T>G XP_024306175.1:n.423-333T>G
NM_006341.4:c.333-333T>G MANE Select NP_006332.3:n.333-333T>G
NM_001127325.2:c.333-333T>G NP_001120797.1:n.333-333T>G