Canonical Allele Identifier: CA035462

Gene: RET

Linked Data

• ClinVar Variation Id: 1596985
• ClinVar RCV Id: RCV002117523
• dbSNP Id: rs376709486
• ExAC: 10:43608991 C / T
• gnomAD v2: 10-43608991-C-T
• gnomAD v3: 10-43113543-C-T
• gnomAD v4: 10-43113543-C-T
• MyVariant Identifiers: chr10:g.43608991C>T (hg19) ; chr10:g.43113543C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113543C>T , CM000672.2:g.43113543C>T	GRCh38
NC_000010.10:g.43608991C>T , CM000672.1:g.43608991C>T	GRCh37
NC_000010.9:g.42928997C>T	NCBI36
NG_007489.1:g.41475C>T , LRG_518:g.41475C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1364-13C>T	ENSP00000480088.2:n.1364-13C>T
ENST00000683007.1:n.1334-13C>T
ENST00000683872.1:n.521-13C>T
ENST00000340058.6:c.1760-13C>T	ENSP00000344798.4:n.1760-13C>T
ENST00000355710.8:c.1760-13C>T MANE Select	ENSP00000347942.3:n.1760-13C>T
ENST00000671844.1:c.*354-13C>T	ENSP00000500541.1:n.*354-13C>T
ENST00000672389.1:c.*354-13C>T	ENSP00000500252.1:n.*354-13C>T
ENST00000340058.5:c.1760-13C>T	ENSP00000344798.4:n.1760-13C>T
ENST00000355710.7:c.1760-13C>T	ENSP00000347942.3:n.1760-13C>T
ENST00000498820.5:c.311-13C>T	ENSP00000419080.1:n.311-13C>T
ENST00000615310.4:c.1289+2311C>T	ENSP00000480088.1:n.1289+2311C>T
NM_020630.4:c.1760-13C>T , LRG_518t2:c.1760-13C>T	NP_065681.1:n.1760-13C>T
NM_020975.4:c.1760-13C>T , LRG_518t1:c.1760-13C>T	NP_066124.1:n.1760-13C>T
XM_011540027.1:c.1760-13C>T	XP_011538329.1:n.1760-13C>T
NM_001355216.1:c.998-13C>T	NP_001342145.1:n.998-13C>T
NM_020630.5:c.1760-13C>T	NP_065681.1:n.1760-13C>T
NM_020975.5:c.1760-13C>T	NP_066124.1:n.1760-13C>T
NM_020975.6:c.1760-13C>T MANE Select	NP_066124.1:n.1760-13C>T
NM_020630.6:c.1760-13C>T	NP_065681.1:n.1760-13C>T