Canonical Allele Identifier: CA1905809415
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43106192G= , CM000672.2:g.43106192G= GRCh38
NC_000010.10:g.43601640G= , CM000672.1:g.43601640G= GRCh37
NC_000010.9:g.42921646G= NCBI36
NG_007489.1:g.34124G= , LRG_518:g.34124G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.867+999G= ENSP00000480088.2:n.867+999G=
ENST00000683007.1:n.442-184G=
ENST00000340058.6:c.868-184G= ENSP00000344798.4:n.868-184G=
ENST00000355710.8:c.868-184G= MANE Select ENSP00000347942.3:n.868-184G=
ENST00000671844.1:c.625+3563G= ENSP00000500541.1:n.625+3563G=
ENST00000672389.1:c.74-5015G= ENSP00000500252.1:n.74-5015G=
ENST00000340058.5:c.868-184G= ENSP00000344798.4:n.868-184G=
ENST00000355710.7:c.868-184G= ENSP00000347942.3:n.868-184G=
ENST00000479913.1:n.463-184G=
ENST00000498820.5:c.74-5907G= ENSP00000419080.1:n.74-5907G=
ENST00000615310.4:c.868-184G= ENSP00000480088.1:n.868-184G=
NM_020630.4:c.868-184G= , LRG_518t2:c.868-184G= NP_065681.1:n.868-184G=
NM_020975.4:c.868-184G= , LRG_518t1:c.868-184G= NP_066124.1:n.868-184G=
XM_011540027.1:c.868-184G= XP_011538329.1:n.868-184G=
NM_001355216.1:c.106-184G= NP_001342145.1:n.106-184G=
NM_020630.5:c.868-184G= NP_065681.1:n.868-184G=
NM_020975.5:c.868-184G= NP_066124.1:n.868-184G=
NM_020975.6:c.868-184G= MANE Select NP_066124.1:n.868-184G=
NM_020630.6:c.868-184G= NP_065681.1:n.868-184G=