Canonical Allele Identifier: CA469479972

Gene: RET

Linked Data

• dbSNP Id: rs2132853410
• MyVariant Identifiers: chr10:g.43610130G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114682G>C , CM000672.2:g.43114682G>C	GRCh38
NC_000010.10:g.43610130G>C , CM000672.1:g.43610130G>C	GRCh37
NC_000010.9:g.42930136G>C	NCBI36
NG_007489.1:g.42614G>C , LRG_518:g.42614G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1686G>C	ENSP00000480088.2:p.Arg562=
ENST00000683007.1:n.1656G>C
ENST00000683872.1:n.1647G>C
ENST00000340058.6:c.2082G>C	ENSP00000344798.4:p.Arg694=
ENST00000355710.8:c.2082G>C MANE Select	ENSP00000347942.3:p.Arg694=
ENST00000671844.1:c.*676G>C	ENSP00000500541.1:n.*676G>C
ENST00000672389.1:c.*676G>C	ENSP00000500252.1:n.*676G>C
ENST00000340058.5:c.2082G>C	ENSP00000344798.4:p.Arg694=
ENST00000355710.7:c.2082G>C	ENSP00000347942.3:p.Arg694=
ENST00000615310.4:c.1289+3450G>C	ENSP00000480088.1:n.1289+3450G>C
NM_020630.4:c.2082G>C , LRG_518t2:c.2082G>C	NP_065681.1:p.Arg694=
NM_020975.4:c.2082G>C , LRG_518t1:c.2082G>C	NP_066124.1:p.Arg694=
XM_011540027.1:c.2082G>C	XP_011538329.1:p.Arg694=
NM_001355216.1:c.1320G>C	NP_001342145.1:p.Arg440=
NM_020630.5:c.2082G>C	NP_065681.1:p.Arg694=
NM_020975.5:c.2082G>C	NP_066124.1:p.Arg694=
NM_020975.6:c.2082G>C MANE Select	NP_066124.1:p.Arg694=
NM_020630.6:c.2082G>C	NP_065681.1:p.Arg694=