Canonical Allele Identifier: CA469274921

Gene: RET

Linked Data

• MyVariant Identifiers: chr10:g.43572742T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077294T>G , CM000672.2:g.43077294T>G	GRCh38
NC_000010.10:g.43572742T>G , CM000672.1:g.43572742T>G	GRCh37
NC_000010.9:g.42892748T>G	NCBI36
NG_007489.1:g.5226T>G , LRG_518:g.5226T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.36T>G	ENSP00000480088.2:p.Arg12=
ENST00000340058.6:c.36T>G	ENSP00000344798.4:p.Arg12=
ENST00000355710.8:c.36T>G MANE Select	ENSP00000347942.3:p.Arg12=
ENST00000671844.1:c.36T>G	ENSP00000500541.1:p.Arg12=
ENST00000672389.1:c.36T>G	ENSP00000500252.1:p.Arg12=
ENST00000340058.5:c.36T>G	ENSP00000344798.4:p.Arg12=
ENST00000355710.7:c.36T>G	ENSP00000347942.3:p.Arg12=
ENST00000498820.5:c.36T>G	ENSP00000419080.1:p.Arg12=
ENST00000615310.4:c.36T>G	ENSP00000480088.1:p.Arg12=
NM_020630.4:c.36T>G , LRG_518t2:c.36T>G	NP_065681.1:p.Arg12=
NM_020975.4:c.36T>G , LRG_518t1:c.36T>G	NP_066124.1:p.Arg12=
XM_011540027.1:c.36T>G	XP_011538329.1:p.Arg12=
NM_020630.5:c.36T>G	NP_065681.1:p.Arg12=
NM_020975.5:c.36T>G	NP_066124.1:p.Arg12=
NM_020975.6:c.36T>G MANE Select	NP_066124.1:p.Arg12=
NM_020630.6:c.36T>G	NP_065681.1:p.Arg12=