Canonical Allele Identifier: CA1153748307
Gene: MAD2L2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11676492G= , CM000663.2:g.11676492G= GRCh38
NC_000001.10:g.11736549G= , CM000663.1:g.11736549G= GRCh37
NC_000001.9:g.11659136G= NCBI36
NG_052907.1:g.20297C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376664.11:n.448-352C=
ENST00000456915.2:c.333-352C= ENSP00000400982.2:n.333-352C=
ENST00000697273.1:c.*152-352C= ENSP00000513220.1:n.*152-352C=
ENST00000697274.1:c.333-352C= ENSP00000513221.1:n.333-352C=
ENST00000376692.9:c.333-352C= MANE Select ENSP00000365882.4:n.333-352C=
ENST00000235310.7:c.333-352C= ENSP00000235310.2:n.333-352C=
ENST00000376664.10:n.418-352C=
ENST00000376667.7:c.333-352C= ENSP00000365855.3:n.333-352C=
ENST00000376669.9:c.371+317C= ENSP00000365857.5:n.371+317C=
ENST00000376672.5:c.371+317C= ENSP00000365860.1:n.371+317C=
ENST00000376692.8:c.333-352C= ENSP00000365882.4:n.333-352C=
ENST00000445656.5:c.423-352C= ENSP00000411807.1:n.423-352C=
ENST00000456915.1:c.333-352C= ENSP00000400982.1:n.333-352C=
NM_001127325.1:c.333-352C= NP_001120797.1:n.333-352C=
NM_006341.3:c.333-352C= NP_006332.3:n.333-352C=
XM_011540507.1:c.333-352C= XP_011538809.1:n.333-352C=
XM_024450407.1:c.423-352C= XP_024306175.1:n.423-352C=
NM_006341.4:c.333-352C= MANE Select NP_006332.3:n.333-352C=
NM_001127325.2:c.333-352C= NP_001120797.1:n.333-352C=