Canonical Allele Identifier: CA206267851

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43126688C>G , CM000672.2:g.43126688C>G	GRCh38
NC_000010.10:g.43622136C>G , CM000672.1:g.43622136C>G	GRCh37
NC_000010.9:g.42942142C>G	NCBI36
NG_007489.1:g.54620C>G , LRG_518:g.54620C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.3153C>G MANE Select	NP_066124.1:p.Ala1051=
ENST00000355710.8:c.3153C>G MANE Select	ENSP00000347942.3:p.Ala1051=
NM_001355216.1:c.2391C>G	NP_001342145.1:p.Ala797=
NM_020630.4:c.3153C>G , LRG_518t2:c.3153C>G	NP_065681.1:p.Ala1051=
NM_020630.5:c.3153C>G	NP_065681.1:p.Ala1051=
NM_020630.6:c.3153C>G	NP_065681.1:p.Ala1051=
NM_020975.4:c.3153C>G , LRG_518t1:c.3153C>G	NP_066124.1:p.Ala1051=
NM_020975.5:c.3153C>G	NP_066124.1:p.Ala1051=
ENST00000340058.5:c.3153C>G	ENSP00000344798.4:p.Ala1051=
ENST00000340058.6:c.3153C>G	ENSP00000344798.4:p.Ala1051=
ENST00000355710.7:c.3153C>G	ENSP00000347942.3:p.Ala1051=
ENST00000615310.4:c.*502C>G	ENSP00000480088.1:n.*502C>G
ENST00000615310.5:c.2757C>G	ENSP00000480088.2:p.Ala919=
ENST00000671844.1:c.*1747C>G	ENSP00000500541.1:n.*1747C>G
ENST00000672389.1:c.*1747C>G	ENSP00000500252.1:n.*1747C>G
ENST00000683007.1:n.2727C>G
XM_011540027.1:c.3153C>G	XP_011538329.1:p.Ala1051=