Canonical Allele Identifier: CA469028999

Gene: RET

Linked Data

• dbSNP Id: rs763149032
• MyVariant Identifiers: chr10:g.43615630T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120182T>C , CM000672.2:g.43120182T>C	GRCh38
NC_000010.10:g.43615630T>C , CM000672.1:g.43615630T>C	GRCh37
NC_000010.9:g.42935636T>C	NCBI36
NG_007489.1:g.48114T>C , LRG_518:g.48114T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2313T>C	ENSP00000480088.2:p.Asp771=
ENST00000683007.1:n.2283T>C
ENST00000683872.1:n.2274T>C
ENST00000340058.6:c.2709T>C	ENSP00000344798.4:p.Asp903=
ENST00000355710.8:c.2709T>C MANE Select	ENSP00000347942.3:p.Asp903=
ENST00000671844.1:c.*1303T>C	ENSP00000500541.1:n.*1303T>C
ENST00000672389.1:c.*1303T>C	ENSP00000500252.1:n.*1303T>C
ENST00000340058.5:c.2709T>C	ENSP00000344798.4:p.Asp903=
ENST00000355710.7:c.2709T>C	ENSP00000347942.3:p.Asp903=
ENST00000615310.4:c.*58T>C	ENSP00000480088.1:n.*58T>C
NM_020630.4:c.2709T>C , LRG_518t2:c.2709T>C	NP_065681.1:p.Asp903=
NM_020975.4:c.2709T>C , LRG_518t1:c.2709T>C	NP_066124.1:p.Asp903=
XM_011540027.1:c.2709T>C	XP_011538329.1:p.Asp903=
NM_001355216.1:c.1947T>C	NP_001342145.1:p.Asp649=
NM_020630.5:c.2709T>C	NP_065681.1:p.Asp903=
NM_020975.5:c.2709T>C	NP_066124.1:p.Asp903=
NM_020975.6:c.2709T>C MANE Select	NP_066124.1:p.Asp903=
NM_020630.6:c.2709T>C	NP_065681.1:p.Asp903=