Canonical Allele Identifier: CA376557261

Gene: RET

Linked Data

• MyVariant Identifiers: chr10:g.43615624A>C (hg19) ; chr10:g.43120176A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120176A>C , CM000672.2:g.43120176A>C	GRCh38
NC_000010.10:g.43615624A>C , CM000672.1:g.43615624A>C	GRCh37
NC_000010.9:g.42935630A>C	NCBI36
NG_007489.1:g.48108A>C , LRG_518:g.48108A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2307A>C	ENSP00000480088.2:p.Glu769Asp
ENST00000683007.1:n.2277A>C
ENST00000683872.1:n.2268A>C
ENST00000340058.6:c.2703A>C	ENSP00000344798.4:p.Glu901Asp
ENST00000355710.8:c.2703A>C MANE Select	ENSP00000347942.3:p.Glu901Asp
ENST00000671844.1:c.*1297A>C	ENSP00000500541.1:n.*1297A>C
ENST00000672389.1:c.*1297A>C	ENSP00000500252.1:n.*1297A>C
ENST00000340058.5:c.2703A>C	ENSP00000344798.4:p.Glu901Asp
ENST00000355710.7:c.2703A>C	ENSP00000347942.3:p.Glu901Asp
ENST00000615310.4:c.*52A>C	ENSP00000480088.1:n.*52A>C
NM_020630.4:c.2703A>C , LRG_518t2:c.2703A>C	NP_065681.1:p.Glu901Asp
NM_020975.4:c.2703A>C , LRG_518t1:c.2703A>C	NP_066124.1:p.Glu901Asp
XM_011540027.1:c.2703A>C	XP_011538329.1:p.Glu901Asp
NM_001355216.1:c.1941A>C	NP_001342145.1:p.Glu647Asp
NM_020630.5:c.2703A>C	NP_065681.1:p.Glu901Asp
NM_020975.5:c.2703A>C	NP_066124.1:p.Glu901Asp
NM_020975.6:c.2703A>C MANE Select	NP_066124.1:p.Glu901Asp
NM_020630.6:c.2703A>C	NP_065681.1:p.Glu901Asp