Canonical Allele Identifier: CA007864

Gene: RET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113627T>A , CM000672.2:g.43113627T>A	GRCh38
NC_000010.10:g.43609075T>A , CM000672.1:g.43609075T>A	GRCh37
NC_000010.9:g.42929081T>A	NCBI36
NG_007489.1:g.41559T>A , LRG_518:g.41559T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1435T>A	ENSP00000480088.2:p.Cys479Ser
ENST00000683007.1:n.1405T>A
ENST00000683872.1:n.592T>A
ENST00000340058.6:c.1831T>A	ENSP00000344798.4:p.Cys611Ser
ENST00000355710.8:c.1831T>A MANE Select	ENSP00000347942.3:p.Cys611Ser
ENST00000671844.1:c.*425T>A	ENSP00000500541.1:n.*425T>A
ENST00000672389.1:c.*425T>A	ENSP00000500252.1:n.*425T>A
ENST00000340058.5:c.1831T>A	ENSP00000344798.4:p.Cys611Ser
ENST00000355710.7:c.1831T>A	ENSP00000347942.3:p.Cys611Ser
ENST00000498820.5:c.382T>A	ENSP00000419080.1:p.Cys128Ser
ENST00000615310.4:c.1289+2395T>A	ENSP00000480088.1:n.1289+2395T>A
NM_020630.4:c.1831T>A , LRG_518t2:c.1831T>A	NP_065681.1:p.Cys611Ser
NM_020975.4:c.1831T>A , LRG_518t1:c.1831T>A	NP_066124.1:p.Cys611Ser
XM_011540027.1:c.1831T>A	XP_011538329.1:p.Cys611Ser
NM_001355216.1:c.1069T>A	NP_001342145.1:p.Cys357Ser
NM_020630.5:c.1831T>A	NP_065681.1:p.Cys611Ser
NM_020975.5:c.1831T>A	NP_066124.1:p.Cys611Ser
NM_020975.6:c.1831T>A MANE Select	NP_066124.1:p.Cys611Ser
NM_020630.6:c.1831T>A	NP_065681.1:p.Cys611Ser