Canonical Allele Identifier: CA2608897176

Gene: RET

Linked Data

• gnomAD v4: 10-43130220-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130220G>T , CM000672.2:g.43130220G>T	GRCh38
NC_000010.10:g.43625668G>T , CM000672.1:g.43625668G>T	GRCh37
NC_000010.9:g.42945674G>T	NCBI36
NG_007489.1:g.58152G>T , LRG_518:g.58152G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.*3466G>T	ENSP00000480088.2:n.*3466G>T
ENST00000683007.1:n.6259G>T
ENST00000355710.8:c.*1951G>T MANE Select	ENSP00000347942.3:n.*1951G>T
ENST00000355710.7:c.*1951G>T	ENSP00000347942.3:n.*1951G>T
ENST00000615310.4:c.*2645G>T	ENSP00000480088.1:n.*2645G>T
NM_020975.4:c.*1951G>T , LRG_518t1:c.*1951G>T	NP_066124.1:n.*1951G>T
XM_011540027.1:c.*719G>T	XP_011538329.1:n.*719G>T
NM_020975.5:c.*1951G>T	NP_066124.1:n.*1951G>T
NM_020975.6:c.*1951G>T MANE Select	NP_066124.1:n.*1951G>T