Canonical Allele Identifier: CA2840894657

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113730A>T , CM000672.2:g.43113730A>T	GRCh38
NC_000010.10:g.43609178A>T , CM000672.1:g.43609178A>T	GRCh37
NC_000010.9:g.42929184A>T	NCBI36
NG_007489.1:g.41662A>T , LRG_518:g.41662A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1483+55A>T	ENSP00000480088.2:n.1483+55A>T
ENST00000683007.1:n.1453+55A>T
ENST00000683872.1:n.695A>T
ENST00000340058.6:c.1879+55A>T	ENSP00000344798.4:n.1879+55A>T
ENST00000355710.8:c.1879+55A>T MANE Select	ENSP00000347942.3:n.1879+55A>T
ENST00000671844.1:c.*473+55A>T	ENSP00000500541.1:n.*473+55A>T
ENST00000672389.1:c.*473+55A>T	ENSP00000500252.1:n.*473+55A>T
ENST00000340058.5:c.1879+55A>T	ENSP00000344798.4:n.1879+55A>T
ENST00000355710.7:c.1879+55A>T	ENSP00000347942.3:n.1879+55A>T
ENST00000498820.5:c.430+55A>T	ENSP00000419080.1:n.430+55A>T
ENST00000615310.4:c.1289+2498A>T	ENSP00000480088.1:n.1289+2498A>T
NM_020630.4:c.1879+55A>T , LRG_518t2:c.1879+55A>T	NP_065681.1:n.1879+55A>T
NM_020975.4:c.1879+55A>T , LRG_518t1:c.1879+55A>T	NP_066124.1:n.1879+55A>T
XM_011540027.1:c.1879+55A>T	XP_011538329.1:n.1879+55A>T
NM_001355216.1:c.1117+55A>T	NP_001342145.1:n.1117+55A>T
NM_020630.5:c.1879+55A>T	NP_065681.1:n.1879+55A>T
NM_020975.5:c.1879+55A>T	NP_066124.1:n.1879+55A>T
NM_020975.6:c.1879+55A>T MANE Select	NP_066124.1:n.1879+55A>T
NM_020630.6:c.1879+55A>T	NP_065681.1:n.1879+55A>T