Canonical Allele Identifier: CA469023531

Gene: RET

Linked Data

• MyVariant Identifiers: chr10:g.43601842C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106394C>T , CM000672.2:g.43106394C>T	GRCh38
NC_000010.10:g.43601842C>T , CM000672.1:g.43601842C>T	GRCh37
NC_000010.9:g.42921848C>T	NCBI36
NG_007489.1:g.34326C>T , LRG_518:g.34326C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.867+1201C>T	ENSP00000480088.2:n.867+1201C>T
ENST00000683007.1:n.460C>T
ENST00000340058.6:c.886C>T	ENSP00000344798.4:p.Leu296=
ENST00000355710.8:c.886C>T MANE Select	ENSP00000347942.3:p.Leu296=
ENST00000671844.1:c.625+3765C>T	ENSP00000500541.1:n.625+3765C>T
ENST00000672389.1:c.74-4813C>T	ENSP00000500252.1:n.74-4813C>T
ENST00000340058.5:c.886C>T	ENSP00000344798.4:p.Leu296=
ENST00000355710.7:c.886C>T	ENSP00000347942.3:p.Leu296=
ENST00000479913.1:n.481C>T
ENST00000498820.5:c.74-5705C>T	ENSP00000419080.1:n.74-5705C>T
ENST00000615310.4:c.886C>T	ENSP00000480088.1:p.Leu296=
NM_020630.4:c.886C>T , LRG_518t2:c.886C>T	NP_065681.1:p.Leu296=
NM_020975.4:c.886C>T , LRG_518t1:c.886C>T	NP_066124.1:p.Leu296=
XM_011540027.1:c.886C>T	XP_011538329.1:p.Leu296=
NM_001355216.1:c.124C>T	NP_001342145.1:p.Leu42=
NM_020630.5:c.886C>T	NP_065681.1:p.Leu296=
NM_020975.5:c.886C>T	NP_066124.1:p.Leu296=
NM_020975.6:c.886C>T MANE Select	NP_066124.1:p.Leu296=
NM_020630.6:c.886C>T	NP_065681.1:p.Leu296=