Canonical Allele Identifier: CA469029047

Gene: RET

Linked Data

• ClinVar Variation Id: 1651162
• ClinVar RCV Id: RCV002151581
• dbSNP Id: rs1369983912
• MyVariant Identifiers: chr10:g.43615639G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120191G>T , CM000672.2:g.43120191G>T	GRCh38
NC_000010.10:g.43615639G>T , CM000672.1:g.43615639G>T	GRCh37
NC_000010.9:g.42935645G>T	NCBI36
NG_007489.1:g.48123G>T , LRG_518:g.48123G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2322G>T	ENSP00000480088.2:p.Val774=
ENST00000683007.1:n.2292G>T
ENST00000683872.1:n.2283G>T
ENST00000340058.6:c.2718G>T	ENSP00000344798.4:p.Val906=
ENST00000355710.8:c.2718G>T MANE Select	ENSP00000347942.3:p.Val906=
ENST00000671844.1:c.*1312G>T	ENSP00000500541.1:n.*1312G>T
ENST00000672389.1:c.*1312G>T	ENSP00000500252.1:n.*1312G>T
ENST00000340058.5:c.2718G>T	ENSP00000344798.4:p.Val906=
ENST00000355710.7:c.2718G>T	ENSP00000347942.3:p.Val906=
ENST00000615310.4:c.*67G>T	ENSP00000480088.1:n.*67G>T
NM_020630.4:c.2718G>T , LRG_518t2:c.2718G>T	NP_065681.1:p.Val906=
NM_020975.4:c.2718G>T , LRG_518t1:c.2718G>T	NP_066124.1:p.Val906=
XM_011540027.1:c.2718G>T	XP_011538329.1:p.Val906=
NM_001355216.1:c.1956G>T	NP_001342145.1:p.Val652=
NM_020630.5:c.2718G>T	NP_065681.1:p.Val906=
NM_020975.5:c.2718G>T	NP_066124.1:p.Val906=
NM_020975.6:c.2718G>T MANE Select	NP_066124.1:p.Val906=
NM_020630.6:c.2718G>T	NP_065681.1:p.Val906=