Canonical Allele Identifier: CA2695211979
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43118399_43118402dup , CM000672.2:g.43118399_43118402dup GRCh38
NC_000010.10:g.43613847_43613850dup , CM000672.1:g.43613847_43613850dup GRCh37
NC_000010.9:g.42933853_42933856dup NCBI36
NG_007489.1:g.46331_46334dup , LRG_518:g.46331_46334dup

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1915_1918dup ENSP00000480088.2:p.Leu640ArgfsTer?
ENST00000683007.1:n.1885_1888dup
ENST00000683872.1:n.1876_1879dup
ENST00000340058.6:c.2311_2314dup ENSP00000344798.4:p.Leu772ArgfsTer?
ENST00000355710.8:c.2311_2314dup MANE Select ENSP00000347942.3:p.Leu772ArgfsTer?
ENST00000671844.1:c.*905_*908dup ENSP00000500541.1:n.*905_*908dup
ENST00000672389.1:c.*905_*908dup ENSP00000500252.1:n.*905_*908dup
ENST00000340058.5:c.2311_2314dup ENSP00000344798.4:p.Leu772ArgfsTer?
ENST00000355710.7:c.2311_2314dup ENSP00000347942.3:p.Leu772ArgfsTer?
ENST00000615310.4:c.1290-1303_1290-1300dup ENSP00000480088.1:n.1290-1303_1290-1300du...
NM_020630.4:c.2311_2314dup , LRG_518t2:c.2311_2314dup NP_065681.1:p.Leu772ArgfsTer?
NM_020975.4:c.2311_2314dup , LRG_518t1:c.2311_2314dup NP_066124.1:p.Leu772ArgfsTer?
XM_011540027.1:c.2311_2314dup XP_011538329.1:p.Leu772ArgfsTer?
NM_001355216.1:c.1549_1552dup NP_001342145.1:p.Leu518ArgfsTer?
NM_020630.5:c.2311_2314dup NP_065681.1:p.Leu772ArgfsTer?
NM_020975.5:c.2311_2314dup NP_066124.1:p.Leu772ArgfsTer?
NM_020975.6:c.2311_2314dup MANE Select NP_066124.1:p.Leu772ArgfsTer?
NM_020630.6:c.2311_2314dup NP_065681.1:p.Leu772ArgfsTer?