Canonical Allele Identifier: CA376550273

Gene: RET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43112120G>C , CM000672.2:g.43112120G>C	GRCh38
NC_000010.10:g.43607568G>C , CM000672.1:g.43607568G>C	GRCh37
NC_000010.9:g.42927574G>C	NCBI36
NG_007489.1:g.40052G>C , LRG_518:g.40052G>C

Transcript Alleles

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