Canonical Allele Identifier: CA1905836566
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1837603690

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100071A>T , CM000672.2:g.43100071A>T GRCh38
NC_000010.10:g.43595519A>T , CM000672.1:g.43595519A>T GRCh37
NC_000010.9:g.42915525A>T NCBI36
NG_007489.1:g.28003A>T , LRG_518:g.28003A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.74-388A>T ENSP00000480088.2:n.74-388A>T
ENST00000340058.6:c.74-388A>T ENSP00000344798.4:n.74-388A>T
ENST00000355710.8:c.74-388A>T MANE Select ENSP00000347942.3:n.74-388A>T
ENST00000671844.1:c.74-388A>T ENSP00000500541.1:n.74-388A>T
ENST00000672389.1:c.74-11136A>T ENSP00000500252.1:n.74-11136A>T
ENST00000340058.5:c.74-388A>T ENSP00000344798.4:n.74-388A>T
ENST00000355710.7:c.74-388A>T ENSP00000347942.3:n.74-388A>T
ENST00000498820.5:c.74-12028A>T ENSP00000419080.1:n.74-12028A>T
ENST00000615310.4:c.74-388A>T ENSP00000480088.1:n.74-388A>T
NM_020630.4:c.74-388A>T , LRG_518t2:c.74-388A>T NP_065681.1:n.74-388A>T
NM_020975.4:c.74-388A>T , LRG_518t1:c.74-388A>T NP_066124.1:n.74-388A>T
XM_011540027.1:c.74-388A>T XP_011538329.1:n.74-388A>T
NM_020630.5:c.74-388A>T NP_065681.1:n.74-388A>T
NM_020975.5:c.74-388A>T NP_066124.1:n.74-388A>T
NM_020975.6:c.74-388A>T MANE Select NP_066124.1:n.74-388A>T
NM_020630.6:c.74-388A>T NP_065681.1:n.74-388A>T