Canonical Allele Identifier: CA2608897178

Gene: RET

Linked Data

• gnomAD v4: 10-43130228-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130228C>T , CM000672.2:g.43130228C>T	GRCh38
NC_000010.10:g.43625676C>T , CM000672.1:g.43625676C>T	GRCh37
NC_000010.9:g.42945682C>T	NCBI36
NG_007489.1:g.58160C>T , LRG_518:g.58160C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*3474C>T	ENSP00000480088.2:n.*3474C>T
ENST00000683007.1:n.6267C>T
ENST00000355710.8:c.*1959C>T MANE Select	ENSP00000347942.3:n.*1959C>T
ENST00000355710.7:c.*1959C>T	ENSP00000347942.3:n.*1959C>T
ENST00000615310.4:c.*2653C>T	ENSP00000480088.1:n.*2653C>T
NM_020975.4:c.*1959C>T , LRG_518t1:c.*1959C>T	NP_066124.1:n.*1959C>T
XM_011540027.1:c.*727C>T	XP_011538329.1:n.*727C>T
NM_020975.5:c.*1959C>T	NP_066124.1:n.*1959C>T
NM_020975.6:c.*1959C>T MANE Select	NP_066124.1:n.*1959C>T