Canonical Allele Identifier: CA376545745

Gene: RET

Linked Data

• MyVariant Identifiers: chr10:g.43601853C>G (hg19) ; chr10:g.43106405C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106405C>G , CM000672.2:g.43106405C>G	GRCh38
NC_000010.10:g.43601853C>G , CM000672.1:g.43601853C>G	GRCh37
NC_000010.9:g.42921859C>G	NCBI36
NG_007489.1:g.34337C>G , LRG_518:g.34337C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.867+1212C>G	ENSP00000480088.2:n.867+1212C>G
ENST00000683007.1:n.471C>G
ENST00000340058.6:c.897C>G	ENSP00000344798.4:p.Phe299Leu
ENST00000355710.8:c.897C>G MANE Select	ENSP00000347942.3:p.Phe299Leu
ENST00000671844.1:c.625+3776C>G	ENSP00000500541.1:n.625+3776C>G
ENST00000672389.1:c.74-4802C>G	ENSP00000500252.1:n.74-4802C>G
ENST00000340058.5:c.897C>G	ENSP00000344798.4:p.Phe299Leu
ENST00000355710.7:c.897C>G	ENSP00000347942.3:p.Phe299Leu
ENST00000479913.1:n.492C>G
ENST00000498820.5:c.74-5694C>G	ENSP00000419080.1:n.74-5694C>G
ENST00000615310.4:c.897C>G	ENSP00000480088.1:p.Phe299Leu
NM_020630.4:c.897C>G , LRG_518t2:c.897C>G	NP_065681.1:p.Phe299Leu
NM_020975.4:c.897C>G , LRG_518t1:c.897C>G	NP_066124.1:p.Phe299Leu
XM_011540027.1:c.897C>G	XP_011538329.1:p.Phe299Leu
NM_001355216.1:c.135C>G	NP_001342145.1:p.Phe45Leu
NM_020630.5:c.897C>G	NP_065681.1:p.Phe299Leu
NM_020975.5:c.897C>G	NP_066124.1:p.Phe299Leu
NM_020975.6:c.897C>G MANE Select	NP_066124.1:p.Phe299Leu
NM_020630.6:c.897C>G	NP_065681.1:p.Phe299Leu