Canonical Allele Identifier: CA2740099756

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114482_43114499del , CM000672.2:g.43114482_43114499del	GRCh38
NC_000010.10:g.43609930_43609947del , CM000672.1:g.43609930_43609947del	GRCh37
NC_000010.9:g.42929936_42929953del	NCBI36
NG_007489.1:g.42414_42431del , LRG_518:g.42414_42431del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1486_1503del	ENSP00000480088.2:p.Pro496_Leu501del
ENST00000683007.1:n.1456_1473del
ENST00000683872.1:n.1447_1464del
ENST00000340058.6:c.1882_1899del	ENSP00000344798.4:p.Pro628_Leu633del
ENST00000355710.8:c.1882_1899del MANE Select	ENSP00000347942.3:p.Pro628_Leu633del
ENST00000671844.1:c.*476_*493del	ENSP00000500541.1:n.*476_*493del
ENST00000672389.1:c.*476_*493del	ENSP00000500252.1:n.*476_*493del
ENST00000340058.5:c.1882_1899del	ENSP00000344798.4:p.Pro628_Leu633del
ENST00000355710.7:c.1882_1899del	ENSP00000347942.3:p.Pro628_Leu633del
ENST00000498820.5:c.433_450del	ENSP00000419080.1:p.Pro145_Leu150del
ENST00000615310.4:c.1289+3250_1289+3267del	ENSP00000480088.1:n.1289+3250_1289+3267del
NM_020630.4:c.1882_1899del , LRG_518t2:c.1882_1899del	NP_065681.1:p.Pro628_Leu633del
NM_020975.4:c.1882_1899del , LRG_518t1:c.1882_1899del	NP_066124.1:p.Pro628_Leu633del
XM_011540027.1:c.1882_1899del	XP_011538329.1:p.Pro628_Leu633del
NM_001355216.1:c.1120_1137del	NP_001342145.1:p.Pro374_Leu379del
NM_020630.5:c.1882_1899del	NP_065681.1:p.Pro628_Leu633del
NM_020975.5:c.1882_1899del	NP_066124.1:p.Pro628_Leu633del
NM_020975.6:c.1882_1899del MANE Select	NP_066124.1:p.Pro628_Leu633del
NM_020630.6:c.1882_1899del	NP_065681.1:p.Pro628_Leu633del