Canonical Allele Identifier: CA1905817158

Gene: RET

Linked Data

• dbSNP Id: rs1838111636

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43117986_43117989del , CM000672.2:g.43117986_43117989del	GRCh38
NC_000010.10:g.43613434_43613437del , CM000672.1:g.43613434_43613437del	GRCh37
NC_000010.9:g.42933440_42933443del	NCBI36
NG_007489.1:g.45918_45921del , LRG_518:g.45918_45921del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1889-387_1889-384del	ENSP00000480088.2:n.1889-387_1889-384del
ENST00000683007.1:n.1859-387_1859-384del
ENST00000683872.1:n.1850-387_1850-384del
ENST00000340058.6:c.2285-387_2285-384del	ENSP00000344798.4:n.2285-387_2285-384del
ENST00000355710.8:c.2285-387_2285-384del MANE Select	ENSP00000347942.3:n.2285-387_2285-384del
ENST00000671844.1:c.*879-387_*879-384del	ENSP00000500541.1:n.*879-387_*879-384del
ENST00000672389.1:c.*879-387_*879-384del	ENSP00000500252.1:n.*879-387_*879-384del
ENST00000340058.5:c.2285-387_2285-384del	ENSP00000344798.4:n.2285-387_2285-384del
ENST00000355710.7:c.2285-387_2285-384del	ENSP00000347942.3:n.2285-387_2285-384del
ENST00000615310.4:c.1290-1716_1290-1713del	ENSP00000480088.1:n.1290-1716_1290-1713del
NM_020630.4:c.2285-387_2285-384del , LRG_518t2:c.2285-387_2285-384del	NP_065681.1:n.2285-387_2285-384del
NM_020975.4:c.2285-387_2285-384del , LRG_518t1:c.2285-387_2285-384del	NP_066124.1:n.2285-387_2285-384del
XM_011540027.1:c.2285-387_2285-384del	XP_011538329.1:n.2285-387_2285-384del
NM_001355216.1:c.1523-387_1523-384del	NP_001342145.1:n.1523-387_1523-384del
NM_020630.5:c.2285-387_2285-384del	NP_065681.1:n.2285-387_2285-384del
NM_020975.5:c.2285-387_2285-384del	NP_066124.1:n.2285-387_2285-384del
NM_020975.6:c.2285-387_2285-384del MANE Select	NP_066124.1:n.2285-387_2285-384del
NM_020630.6:c.2285-387_2285-384del	NP_065681.1:n.2285-387_2285-384del