Canonical Allele Identifier: CA1905813476

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114500_43114501delinsTG , CM000672.2:g.43114500_43114501delinsTG	GRCh38
NC_000010.10:g.43609948_43609949delinsTG , CM000672.1:g.43609948_43609949delinsTG	GRCh37
NC_000010.9:g.42929954_42929955delinsTG	NCBI36
NG_007489.1:g.42432_42433delinsTG , LRG_518:g.42432_42433delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1504_1505delinsTG	ENSP00000480088.2:p.Cys502=
ENST00000683007.1:n.1474_1475delinsTG
ENST00000683872.1:n.1465_1466delinsTG
ENST00000340058.6:c.1900_1901delinsTG	ENSP00000344798.4:p.Cys634=
ENST00000355710.8:c.1900_1901delinsTG MANE Select	ENSP00000347942.3:p.Cys634=
ENST00000671844.1:c.*494_*495delinsTG	ENSP00000500541.1:n.*494_*495delinsTG
ENST00000672389.1:c.*494_*495delinsTG	ENSP00000500252.1:n.*494_*495delinsTG
ENST00000340058.5:c.1900_1901delinsTG	ENSP00000344798.4:p.Cys634=
ENST00000355710.7:c.1900_1901delinsTG	ENSP00000347942.3:p.Cys634=
ENST00000498820.5:c.451_452delinsTG	ENSP00000419080.1:p.Cys151=
ENST00000615310.4:c.1289+3268_1289+3269delinsTG	ENSP00000480088.1:n.1289+3268_1289+3269de...
NM_020630.4:c.1900_1901delinsTG , LRG_518t2:c.1900_1901delinsTG	NP_065681.1:p.Cys634=
NM_020975.4:c.1900_1901delinsTG , LRG_518t1:c.1900_1901delinsTG	NP_066124.1:p.Cys634=
XM_011540027.1:c.1900_1901delinsTG	XP_011538329.1:p.Cys634=
NM_001355216.1:c.1138_1139delinsTG	NP_001342145.1:p.Cys380=
NM_020630.5:c.1900_1901delinsTG	NP_065681.1:p.Cys634=
NM_020975.5:c.1900_1901delinsTG	NP_066124.1:p.Cys634=
NM_020975.6:c.1900_1901delinsTG MANE Select	NP_066124.1:p.Cys634=
NM_020630.6:c.1900_1901delinsTG	NP_065681.1:p.Cys634=