Canonical Allele Identifier: CA007894

Gene: RET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113628_43113629delinsAT , CM000672.2:g.43113628_43113629delinsAT	GRCh38
NC_000010.10:g.43609076_43609077delinsAT , CM000672.1:g.43609076_43609077delinsAT	GRCh37
NC_000010.9:g.42929082_42929083delinsAT	NCBI36
NG_007489.1:g.41560_41561delinsAT , LRG_518:g.41560_41561delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1436_1437delinsAT	ENSP00000480088.2:p.Cys479Tyr
ENST00000683007.1:n.1406_1407delinsAT
ENST00000683872.1:n.593_594delinsAT
ENST00000340058.6:c.1832_1833delinsAT	ENSP00000344798.4:p.Cys611Tyr
ENST00000355710.8:c.1832_1833delinsAT MANE Select	ENSP00000347942.3:p.Cys611Tyr
ENST00000671844.1:c.*426_*427delinsAT	ENSP00000500541.1:n.*426_*427delinsAT
ENST00000672389.1:c.*426_*427delinsAT	ENSP00000500252.1:n.*426_*427delinsAT
ENST00000340058.5:c.1832_1833delinsAT	ENSP00000344798.4:p.Cys611Tyr
ENST00000355710.7:c.1832_1833delinsAT	ENSP00000347942.3:p.Cys611Tyr
ENST00000498820.5:c.383_384delinsAT	ENSP00000419080.1:p.Cys128Tyr
ENST00000615310.4:c.1289+2396_1289+2397delinsAT	ENSP00000480088.1:n.1289+2396_1289+2397delinsAT
NM_020630.4:c.1832_1833delinsAT , LRG_518t2:c.1832_1833delinsAT	NP_065681.1:p.Cys611Tyr
NM_020975.4:c.1832_1833delinsAT , LRG_518t1:c.1832_1833delinsAT	NP_066124.1:p.Cys611Tyr
XM_011540027.1:c.1832_1833delinsAT	XP_011538329.1:p.Cys611Tyr
NM_001355216.1:c.1070_1071delinsAT	NP_001342145.1:p.Cys357Tyr
NM_020630.5:c.1832_1833delinsAT	NP_065681.1:p.Cys611Tyr
NM_020975.5:c.1832_1833delinsAT	NP_066124.1:p.Cys611Tyr
NM_020975.6:c.1832_1833delinsAT MANE Select	NP_066124.1:p.Cys611Tyr
NM_020630.6:c.1832_1833delinsAT	NP_065681.1:p.Cys611Tyr