Canonical Allele Identifier: CA2608895991
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43128010-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43128010A>C , CM000672.2:g.43128010A>C GRCh38
NC_000010.10:g.43623458A>C , CM000672.1:g.43623458A>C GRCh37
NC_000010.9:g.42943464A>C NCBI36
NG_007489.1:g.55942A>C , LRG_518:g.55942A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*1256A>C ENSP00000480088.2:n.*1256A>C
ENST00000683007.1:n.4049A>C
ENST00000355710.8:c.3188-102A>C MANE Select ENSP00000347942.3:n.3188-102A>C
ENST00000355710.7:c.3188-102A>C ENSP00000347942.3:n.3188-102A>C
ENST00000615310.4:c.*537-102A>C ENSP00000480088.1:n.*537-102A>C
NM_020975.4:c.3188-102A>C , LRG_518t1:c.3188-102A>C NP_066124.1:n.3188-102A>C
XM_011540027.1:c.3188-102A>C XP_011538329.1:n.3188-102A>C
NM_020975.5:c.3188-102A>C NP_066124.1:n.3188-102A>C
NM_020975.6:c.3188-102A>C MANE Select NP_066124.1:n.3188-102A>C
Search 100 bp 5'
Search 100 bp 3'