Canonical Allele Identifier: CA1905809504
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43106405C= , CM000672.2:g.43106405C= GRCh38
NC_000010.10:g.43601853C= , CM000672.1:g.43601853C= GRCh37
NC_000010.9:g.42921859C= NCBI36
NG_007489.1:g.34337C= , LRG_518:g.34337C=

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.867+1212C= ENSP00000480088.2:n.867+1212C=
ENST00000683007.1:n.471C=
ENST00000340058.6:c.897C= ENSP00000344798.4:p.Phe299=
ENST00000355710.8:c.897C= MANE Select ENSP00000347942.3:p.Phe299=
ENST00000671844.1:c.625+3776C= ENSP00000500541.1:n.625+3776C=
ENST00000672389.1:c.74-4802C= ENSP00000500252.1:n.74-4802C=
ENST00000340058.5:c.897C= ENSP00000344798.4:p.Phe299=
ENST00000355710.7:c.897C= ENSP00000347942.3:p.Phe299=
ENST00000479913.1:n.492C=
ENST00000498820.5:c.74-5694C= ENSP00000419080.1:n.74-5694C=
ENST00000615310.4:c.897C= ENSP00000480088.1:p.Phe299=
NM_020630.4:c.897C= , LRG_518t2:c.897C= NP_065681.1:p.Phe299=
NM_020975.4:c.897C= , LRG_518t1:c.897C= NP_066124.1:p.Phe299=
XM_011540027.1:c.897C= XP_011538329.1:p.Phe299=
NM_001355216.1:c.135C= NP_001342145.1:p.Phe45=
NM_020630.5:c.897C= NP_065681.1:p.Phe299=
NM_020975.5:c.897C= NP_066124.1:p.Phe299=
NM_020975.6:c.897C= MANE Select NP_066124.1:p.Phe299=
NM_020630.6:c.897C= NP_065681.1:p.Phe299=