Canonical Allele Identifier: CA593289993

Gene: RET

Linked Data

• dbSNP Id: rs1564498890
• gnomAD v2: 10-43615237-A-ACACCCTGACCCACCACGCCC
• MyVariant Identifiers: chr10:g.43615237_43615238insCACCCTGACCCACCACGCCC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119791_43119810dup , CM000672.2:g.43119791_43119810dup	GRCh38
NC_000010.10:g.43615239_43615258dup , CM000672.1:g.43615239_43615258dup	GRCh37
NC_000010.9:g.42935245_42935264dup	NCBI36
NG_007489.1:g.47723_47742dup , LRG_518:g.47723_47742dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2211+46_2211+65dup	ENSP00000480088.2:n.2211+46_2211+65dup
ENST00000683007.1:n.2181+46_2181+65dup
ENST00000683872.1:n.2172+46_2172+65dup
ENST00000340058.6:c.2607+46_2607+65dup	ENSP00000344798.4:n.2607+46_2607+65dup
ENST00000355710.8:c.2607+46_2607+65dup MANE Select	ENSP00000347942.3:n.2607+46_2607+65dup
ENST00000671844.1:c.*1201+46_*1201+65dup	ENSP00000500541.1:n.*1201+46_*1201+65dup
ENST00000672389.1:c.*1201+46_*1201+65dup	ENSP00000500252.1:n.*1201+46_*1201+65dup
ENST00000340058.5:c.2607+46_2607+65dup	ENSP00000344798.4:n.2607+46_2607+65dup
ENST00000355710.7:c.2607+46_2607+65dup	ENSP00000347942.3:n.2607+46_2607+65dup
ENST00000615310.4:c.1333+46_1333+65dup	ENSP00000480088.1:n.1333+46_1333+65dup
NM_020630.4:c.2607+46_2607+65dup , LRG_518t2:c.2607+46_2607+65dup	NP_065681.1:n.2607+46_2607+65dup
NM_020975.4:c.2607+46_2607+65dup , LRG_518t1:c.2607+46_2607+65dup	NP_066124.1:n.2607+46_2607+65dup
XM_011540027.1:c.2607+46_2607+65dup	XP_011538329.1:n.2607+46_2607+65dup
NM_001355216.1:c.1845+46_1845+65dup	NP_001342145.1:n.1845+46_1845+65dup
NM_020630.5:c.2607+46_2607+65dup	NP_065681.1:n.2607+46_2607+65dup
NM_020975.5:c.2607+46_2607+65dup	NP_066124.1:n.2607+46_2607+65dup
NM_020975.6:c.2607+46_2607+65dup MANE Select	NP_066124.1:n.2607+46_2607+65dup
NM_020630.6:c.2607+46_2607+65dup	NP_065681.1:n.2607+46_2607+65dup