Canonical Allele Identifier: CA376556969

Gene: RET

Linked Data

• MyVariant Identifiers: chr10:g.43615534T>G (hg19) ; chr10:g.43120086T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120086T>G , CM000672.2:g.43120086T>G	GRCh38
NC_000010.10:g.43615534T>G , CM000672.1:g.43615534T>G	GRCh37
NC_000010.9:g.42935540T>G	NCBI36
NG_007489.1:g.48018T>G , LRG_518:g.48018T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2217T>G	ENSP00000480088.2:p.Val739=
ENST00000683007.1:n.2187T>G
ENST00000683872.1:n.2178T>G
ENST00000340058.6:c.2613T>G	ENSP00000344798.4:p.Val871=
ENST00000355710.8:c.2613T>G MANE Select	ENSP00000347942.3:p.Val871=
ENST00000671844.1:c.*1207T>G	ENSP00000500541.1:n.*1207T>G
ENST00000672389.1:c.*1207T>G	ENSP00000500252.1:n.*1207T>G
ENST00000340058.5:c.2613T>G	ENSP00000344798.4:p.Val871=
ENST00000355710.7:c.2613T>G	ENSP00000347942.3:p.Val871=
ENST00000615310.4:c.1339T>G	ENSP00000480088.1:p.Ser447Ala
NM_020630.4:c.2613T>G , LRG_518t2:c.2613T>G	NP_065681.1:p.Val871=
NM_020975.4:c.2613T>G , LRG_518t1:c.2613T>G	NP_066124.1:p.Val871=
XM_011540027.1:c.2613T>G	XP_011538329.1:p.Val871=
NM_001355216.1:c.1851T>G	NP_001342145.1:p.Val617=
NM_020630.5:c.2613T>G	NP_065681.1:p.Val871=
NM_020975.5:c.2613T>G	NP_066124.1:p.Val871=
NM_020975.6:c.2613T>G MANE Select	NP_066124.1:p.Val871=
NM_020630.6:c.2613T>G	NP_065681.1:p.Val871=