Canonical Allele Identifier: CA469275097

Gene: RET

Linked Data

• ClinVar Variation Id: 1608560
• ClinVar RCV Id: RCV002162957
• dbSNP Id: rs1263991822
• gnomAD v4: 10-43077318-G-A
• MyVariant Identifiers: chr10:g.43572766G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077318G>A , CM000672.2:g.43077318G>A	GRCh38
NC_000010.10:g.43572766G>A , CM000672.1:g.43572766G>A	GRCh37
NC_000010.9:g.42892772G>A	NCBI36
NG_007489.1:g.5250G>A , LRG_518:g.5250G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.60G>A	ENSP00000480088.2:p.Pro20=
ENST00000340058.6:c.60G>A	ENSP00000344798.4:p.Pro20=
ENST00000355710.8:c.60G>A MANE Select	ENSP00000347942.3:p.Pro20=
ENST00000671844.1:c.60G>A	ENSP00000500541.1:p.Pro20=
ENST00000672389.1:c.60G>A	ENSP00000500252.1:p.Pro20=
ENST00000340058.5:c.60G>A	ENSP00000344798.4:p.Pro20=
ENST00000355710.7:c.60G>A	ENSP00000347942.3:p.Pro20=
ENST00000498820.5:c.60G>A	ENSP00000419080.1:p.Pro20=
ENST00000615310.4:c.60G>A	ENSP00000480088.1:p.Pro20=
NM_020630.4:c.60G>A , LRG_518t2:c.60G>A	NP_065681.1:p.Pro20=
NM_020975.4:c.60G>A , LRG_518t1:c.60G>A	NP_066124.1:p.Pro20=
XM_011540027.1:c.60G>A	XP_011538329.1:p.Pro20=
NM_020630.5:c.60G>A	NP_065681.1:p.Pro20=
NM_020975.5:c.60G>A	NP_066124.1:p.Pro20=
NM_020975.6:c.60G>A MANE Select	NP_066124.1:p.Pro20=
NM_020630.6:c.60G>A	NP_065681.1:p.Pro20=