Canonical Allele Identifier: CA1905819687
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1838171229

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119922_43119923del , CM000672.2:g.43119922_43119923del GRCh38
NC_000010.10:g.43615370_43615371del , CM000672.1:g.43615370_43615371del GRCh37
NC_000010.9:g.42935376_42935377del NCBI36
NG_007489.1:g.47854_47855del , LRG_518:g.47854_47855del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.2212-159_2212-158del ENSP00000480088.2:n.2212-159_2212-158del
ENST00000683007.1:n.2182-159_2182-158del
ENST00000683872.1:n.2173-159_2173-158del
ENST00000340058.6:c.2608-159_2608-158del ENSP00000344798.4:n.2608-159_2608-158del
ENST00000355710.8:c.2608-159_2608-158del MANE Select ENSP00000347942.3:n.2608-159_2608-158del
ENST00000671844.1:c.*1202-159_*1202-158del ENSP00000500541.1:n.*1202-159_*1202-158del
ENST00000672389.1:c.*1202-159_*1202-158del ENSP00000500252.1:n.*1202-159_*1202-158del
ENST00000340058.5:c.2608-159_2608-158del ENSP00000344798.4:n.2608-159_2608-158del
ENST00000355710.7:c.2608-159_2608-158del ENSP00000347942.3:n.2608-159_2608-158del
ENST00000615310.4:c.1334-159_1334-158del ENSP00000480088.1:n.1334-159_1334-158del
NM_020630.4:c.2608-159_2608-158del , LRG_518t2:c.2608-159_2608-158del NP_065681.1:n.2608-159_2608-158del
NM_020975.4:c.2608-159_2608-158del , LRG_518t1:c.2608-159_2608-158del NP_066124.1:n.2608-159_2608-158del
XM_011540027.1:c.2608-159_2608-158del XP_011538329.1:n.2608-159_2608-158del
NM_001355216.1:c.1846-159_1846-158del NP_001342145.1:n.1846-159_1846-158del
NM_020630.5:c.2608-159_2608-158del NP_065681.1:n.2608-159_2608-158del
NM_020975.5:c.2608-159_2608-158del NP_066124.1:n.2608-159_2608-158del
NM_020975.6:c.2608-159_2608-158del MANE Select NP_066124.1:n.2608-159_2608-158del
NM_020630.6:c.2608-159_2608-158del NP_065681.1:n.2608-159_2608-158del