Canonical Allele Identifier: CA1905819646

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119880_43119881delinsCA , CM000672.2:g.43119880_43119881delinsCA	GRCh38
NC_000010.10:g.43615328_43615329delinsCA , CM000672.1:g.43615328_43615329delinsCA	GRCh37
NC_000010.9:g.42935334_42935335delinsCA	NCBI36
NG_007489.1:g.47812_47813delinsCA , LRG_518:g.47812_47813delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+135_2211+136delinsCA	ENSP00000480088.2:n.2211+135_2211+136delinsCA
ENST00000683007.1:n.2181+135_2181+136delinsCA
ENST00000683872.1:n.2172+135_2172+136delinsCA
ENST00000340058.6:c.2607+135_2607+136delinsCA	ENSP00000344798.4:n.2607+135_2607+136delinsCA
ENST00000355710.8:c.2607+135_2607+136delinsCA MANE Select	ENSP00000347942.3:n.2607+135_2607+136delinsCA
ENST00000671844.1:c.*1201+135_*1201+136delinsCA	ENSP00000500541.1:n.*1201+135_*1201+136delinsCA
ENST00000672389.1:c.*1201+135_*1201+136delinsCA	ENSP00000500252.1:n.*1201+135_*1201+136delinsCA
ENST00000340058.5:c.2607+135_2607+136delinsCA	ENSP00000344798.4:n.2607+135_2607+136delinsCA
ENST00000355710.7:c.2607+135_2607+136delinsCA	ENSP00000347942.3:n.2607+135_2607+136delinsCA
ENST00000615310.4:c.1333+135_1333+136delinsCA	ENSP00000480088.1:n.1333+135_1333+136delinsCA
NM_020630.4:c.2607+135_2607+136delinsCA , LRG_518t2:c.2607+135_2607+136delinsCA	NP_065681.1:n.2607+135_2607+136delinsCA
NM_020975.4:c.2607+135_2607+136delinsCA , LRG_518t1:c.2607+135_2607+136delinsCA	NP_066124.1:n.2607+135_2607+136delinsCA
XM_011540027.1:c.2607+135_2607+136delinsCA	XP_011538329.1:n.2607+135_2607+136delinsCA
NM_001355216.1:c.1845+135_1845+136delinsCA	NP_001342145.1:n.1845+135_1845+136delinsCA
NM_020630.5:c.2607+135_2607+136delinsCA	NP_065681.1:n.2607+135_2607+136delinsCA
NM_020975.5:c.2607+135_2607+136delinsCA	NP_066124.1:n.2607+135_2607+136delinsCA
NM_020975.6:c.2607+135_2607+136delinsCA MANE Select	NP_066124.1:n.2607+135_2607+136delinsCA
NM_020630.6:c.2607+135_2607+136delinsCA	NP_065681.1:n.2607+135_2607+136delinsCA