Canonical Allele Identifier: CA1905814005
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077074C= , CM000672.2:g.43077074C= GRCh38
NC_000010.10:g.43572522C= , CM000672.1:g.43572522C= GRCh37
NC_000010.9:g.42892528C= NCBI36
NG_007489.1:g.5006C= , LRG_518:g.5006C=

Transcript Alleles

HGVS Amino-acid change
ENST00000340058.6:c.-185C= ENSP00000344798.4:n.-185C=
ENST00000355710.8:c.-185C= MANE Select ENSP00000347942.3:n.-185C=
ENST00000671844.1:c.-185C= ENSP00000500541.1:n.-185C=
ENST00000672389.1:c.-185C= ENSP00000500252.1:n.-185C=
ENST00000355710.7:c.-185C= ENSP00000347942.3:n.-185C=
ENST00000498820.5:c.-185C= ENSP00000419080.1:n.-185C=
ENST00000615310.4:c.-185C= ENSP00000480088.1:n.-185C=
NM_020630.4:c.-185C= , LRG_518t2:c.-185C= NP_065681.1:n.-185C=
NM_020975.4:c.-185C= , LRG_518t1:c.-185C= NP_066124.1:n.-185C=
XM_011540027.1:c.-185C= XP_011538329.1:n.-185C=
NM_020630.5:c.-185C= NP_065681.1:n.-185C=
NM_020975.5:c.-185C= NP_066124.1:n.-185C=
NM_020975.6:c.-185C= MANE Select NP_066124.1:n.-185C=
NM_020630.6:c.-185C= NP_065681.1:n.-185C=