Canonical Allele Identifier: CA1905813063

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113635_43113638delinsTGAG , CM000672.2:g.43113635_43113638delinsTGAG	GRCh38
NC_000010.10:g.43609083_43609086delinsTGAG , CM000672.1:g.43609083_43609086delinsTGAG	GRCh37
NC_000010.9:g.42929089_42929092delinsTGAG	NCBI36
NG_007489.1:g.41567_41570delinsTGAG , LRG_518:g.41567_41570delinsTGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1443_1446delinsTGAG	ENSP00000480088.2:p.Pro481=
ENST00000683007.1:n.1413_1416delinsTGAG
ENST00000683872.1:n.600_603delinsTGAG
ENST00000340058.6:c.1839_1842delinsTGAG	ENSP00000344798.4:p.Pro613=
ENST00000355710.8:c.1839_1842delinsTGAG MANE Select	ENSP00000347942.3:p.Pro613=
ENST00000671844.1:c.*433_*436delinsTGAG	ENSP00000500541.1:n.*433_*436delinsTGAG
ENST00000672389.1:c.*433_*436delinsTGAG	ENSP00000500252.1:n.*433_*436delinsTGAG
ENST00000340058.5:c.1839_1842delinsTGAG	ENSP00000344798.4:p.Pro613=
ENST00000355710.7:c.1839_1842delinsTGAG	ENSP00000347942.3:p.Pro613=
ENST00000498820.5:c.390_393delinsTGAG	ENSP00000419080.1:p.Pro130=
ENST00000615310.4:c.1289+2403_1289+2406delinsTGAG	ENSP00000480088.1:n.1289+2403_1289+2406de...
NM_020630.4:c.1839_1842delinsTGAG , LRG_518t2:c.1839_1842delinsTGAG	NP_065681.1:p.Pro613=
NM_020975.4:c.1839_1842delinsTGAG , LRG_518t1:c.1839_1842delinsTGAG	NP_066124.1:p.Pro613=
XM_011540027.1:c.1839_1842delinsTGAG	XP_011538329.1:p.Pro613=
NM_001355216.1:c.1077_1080delinsTGAG	NP_001342145.1:p.Pro359=
NM_020630.5:c.1839_1842delinsTGAG	NP_065681.1:p.Pro613=
NM_020975.5:c.1839_1842delinsTGAG	NP_066124.1:p.Pro613=
NM_020975.6:c.1839_1842delinsTGAG MANE Select	NP_066124.1:p.Pro613=
NM_020630.6:c.1839_1842delinsTGAG	NP_065681.1:p.Pro613=