Canonical Allele Identifier: CA376552900

Gene: RET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114491G>C , CM000672.2:g.43114491G>C	GRCh38
NC_000010.10:g.43609939G>C , CM000672.1:g.43609939G>C	GRCh37
NC_000010.9:g.42929945G>C	NCBI36
NG_007489.1:g.42423G>C , LRG_518:g.42423G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1495G>C	ENSP00000480088.2:p.Asp499His
ENST00000683007.1:n.1465G>C
ENST00000683872.1:n.1456G>C
ENST00000340058.6:c.1891G>C	ENSP00000344798.4:p.Asp631His
ENST00000355710.8:c.1891G>C MANE Select	ENSP00000347942.3:p.Asp631His
ENST00000671844.1:c.*485G>C	ENSP00000500541.1:n.*485G>C
ENST00000672389.1:c.*485G>C	ENSP00000500252.1:n.*485G>C
ENST00000340058.5:c.1891G>C	ENSP00000344798.4:p.Asp631His
ENST00000355710.7:c.1891G>C	ENSP00000347942.3:p.Asp631His
ENST00000498820.5:c.442G>C	ENSP00000419080.1:p.Asp148His
ENST00000615310.4:c.1289+3259G>C	ENSP00000480088.1:n.1289+3259G>C
NM_020630.4:c.1891G>C , LRG_518t2:c.1891G>C	NP_065681.1:p.Asp631His
NM_020975.4:c.1891G>C , LRG_518t1:c.1891G>C	NP_066124.1:p.Asp631His
XM_011540027.1:c.1891G>C	XP_011538329.1:p.Asp631His
NM_001355216.1:c.1129G>C	NP_001342145.1:p.Asp377His
NM_020630.5:c.1891G>C	NP_065681.1:p.Asp631His
NM_020975.5:c.1891G>C	NP_066124.1:p.Asp631His
NM_020975.6:c.1891G>C MANE Select	NP_066124.1:p.Asp631His
NM_020630.6:c.1891G>C	NP_065681.1:p.Asp631His