Canonical Allele Identifier: CA2580615458

Gene: RET

Linked Data

• ClinVar Variation Id: 2573246
• ClinVar RCV Id: RCV003316935

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118392_43118395delinsCCTT , CM000672.2:g.43118392_43118395delinsCCTT	GRCh38
NC_000010.10:g.43613840_43613843delinsCCTT , CM000672.1:g.43613840_43613843delinsCCTT	GRCh37
NC_000010.9:g.42933846_42933849delinsCCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1908_1911delinsCCTT	ENSP00000480088.2:p.Glu636Asp
ENST00000683007.1:n.1878_1881delinsCCTT
ENST00000683872.1:n.1869_1872delinsCCTT
ENST00000340058.6:c.2304_2307delinsCCTT	ENSP00000344798.4:p.Glu768Asp
ENST00000355710.8:c.2304_2307delinsCCTT MANE Select	ENSP00000347942.3:p.Glu768Asp
ENST00000671844.1:c.*898_*901delinsCCTT	ENSP00000500541.1:n.*898_*901delinsCCTT
ENST00000672389.1:c.*898_*901delinsCCTT	ENSP00000500252.1:n.*898_*901delinsCCTT
ENST00000340058.5:c.2304_2307delinsCCTT	ENSP00000344798.4:p.Glu768Asp
ENST00000355710.7:c.2304_2307delinsCCTT	ENSP00000347942.3:p.Glu768Asp
ENST00000615310.4:c.1290-1310_1290-1307delinsCCTT	ENSP00000480088.1:n.1290-1310_1290-1307de...
XM_011540027.1:c.2304_2307delinsCCTT	XP_011538329.1:p.Glu768Asp
NM_001355216.1:c.1542_1545delinsCCTT	NP_001342145.1:p.Glu514Asp
NM_020630.5:c.2304_2307delinsCCTT	NP_065681.1:p.Glu768Asp
NM_020975.5:c.2304_2307delinsCCTT	NP_066124.1:p.Glu768Asp
NM_020975.6:c.2304_2307delinsCCTT MANE Select	NP_066124.1:p.Glu768Asp
NM_020630.6:c.2304_2307delinsCCTT	NP_065681.1:p.Glu768Asp