Canonical Allele Identifier: CA2608897167

Gene: RET

Linked Data

• gnomAD v4: 10-43130171-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130171T>C , CM000672.2:g.43130171T>C	GRCh38
NC_000010.10:g.43625619T>C , CM000672.1:g.43625619T>C	GRCh37
NC_000010.9:g.42945625T>C	NCBI36
NG_007489.1:g.58103T>C , LRG_518:g.58103T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*3417T>C	ENSP00000480088.2:n.*3417T>C
ENST00000683007.1:n.6210T>C
ENST00000355710.8:c.*1902T>C MANE Select	ENSP00000347942.3:n.*1902T>C
ENST00000355710.7:c.*1902T>C	ENSP00000347942.3:n.*1902T>C
ENST00000615310.4:c.*2596T>C	ENSP00000480088.1:n.*2596T>C
NM_020975.4:c.*1902T>C , LRG_518t1:c.*1902T>C	NP_066124.1:n.*1902T>C
XM_011540027.1:c.*670T>C	XP_011538329.1:n.*670T>C
NM_020975.5:c.*1902T>C	NP_066124.1:n.*1902T>C
NM_020975.6:c.*1902T>C MANE Select	NP_066124.1:n.*1902T>C