Allele Registry

Canonical Allele Identifier: CA007626

Gene: RET HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr10:g.43112120_43112121delinsCT

GRCh37 chr10:g.43607568_43607569delinsCT

Linked Data - NCBI & NCI

dbSNP:

377767389

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43112120_43112121delinsCT , CM000672.2:g.43112120_43112121delinsCT	GRCh38
NC_000010.10:g.43607568_43607569delinsCT , CM000672.1:g.43607568_43607569delinsCT	GRCh37
NC_000010.9:g.42927574_42927575delinsCT	NCBI36
NG_007489.1:g.40052_40053delinsCT , LRG_518:g.40052_40053delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1148_1149delinsCT	ENSP00000480088.2:p.Cys383Ser
ENST00000683007.1:n.1118_1119delinsCT
ENST00000683872.1:n.305_306delinsCT
ENST00000340058.6:c.1544_1545delinsCT	ENSP00000344798.4:p.Cys515Ser
ENST00000355710.8:c.1544_1545delinsCT MANE Select	ENSP00000347942.3:p.Cys515Ser
ENST00000671844.1:c.138_139delinsCT	ENSP00000500541.1:n.138_139delinsCT
ENST00000672389.1:c.138_139delinsCT	ENSP00000500252.1:n.138_139delinsCT
ENST00000340058.5:c.1544_1545delinsCT	ENSP00000344798.4:p.Cys515Ser
ENST00000355710.7:c.1544_1545delinsCT	ENSP00000347942.3:p.Cys515Ser
ENST00000498820.5:c.95_96delinsCT	ENSP00000419080.1:p.Cys32Ser
ENST00000615310.4:c.1289+888_1289+889delinsCT	ENSP00000480088.1:n.1289+888_1289+889delinsCT
NM_020630.4:c.1544_1545delinsCT , LRG_518t2:c.1544_1545delinsCT	NP_065681.1:p.Cys515Ser
NM_020975.4:c.1544_1545delinsCT , LRG_518t1:c.1544_1545delinsCT	NP_066124.1:p.Cys515Ser
XM_011540027.1:c.1544_1545delinsCT	XP_011538329.1:p.Cys515Ser
NM_001355216.1:c.782_783delinsCT	NP_001342145.1:p.Cys261Ser
NM_020630.5:c.1544_1545delinsCT	NP_065681.1:p.Cys515Ser
NM_020975.5:c.1544_1545delinsCT	NP_066124.1:p.Cys515Ser
NM_020975.6:c.1544_1545delinsCT MANE Select	NP_066124.1:p.Cys515Ser
NM_020630.6:c.1544_1545delinsCT	NP_065681.1:p.Cys515Ser

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