Canonical Allele Identifier: CA1905813462
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43114492A= , CM000672.2:g.43114492A= GRCh38
NC_000010.10:g.43609940A= , CM000672.1:g.43609940A= GRCh37
NC_000010.9:g.42929946A= NCBI36
NG_007489.1:g.42424A= , LRG_518:g.42424A=

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1496A= ENSP00000480088.2:p.Asp499=
ENST00000683007.1:n.1466A=
ENST00000683872.1:n.1457A=
ENST00000340058.6:c.1892A= ENSP00000344798.4:p.Asp631=
ENST00000355710.8:c.1892A= MANE Select ENSP00000347942.3:p.Asp631=
ENST00000671844.1:c.*486A= ENSP00000500541.1:n.*486A=
ENST00000672389.1:c.*486A= ENSP00000500252.1:n.*486A=
ENST00000340058.5:c.1892A= ENSP00000344798.4:p.Asp631=
ENST00000355710.7:c.1892A= ENSP00000347942.3:p.Asp631=
ENST00000498820.5:c.443A= ENSP00000419080.1:p.Asp148=
ENST00000615310.4:c.1289+3260A= ENSP00000480088.1:n.1289+3260A=
NM_020630.4:c.1892A= , LRG_518t2:c.1892A= NP_065681.1:p.Asp631=
NM_020975.4:c.1892A= , LRG_518t1:c.1892A= NP_066124.1:p.Asp631=
XM_011540027.1:c.1892A= XP_011538329.1:p.Asp631=
NM_001355216.1:c.1130A= NP_001342145.1:p.Asp377=
NM_020630.5:c.1892A= NP_065681.1:p.Asp631=
NM_020975.5:c.1892A= NP_066124.1:p.Asp631=
NM_020975.6:c.1892A= MANE Select NP_066124.1:p.Asp631=
NM_020630.6:c.1892A= NP_065681.1:p.Asp631=