Canonical Allele Identifier: CA1905819918

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120144T= , CM000672.2:g.43120144T=	GRCh38
NC_000010.10:g.43615592T= , CM000672.1:g.43615592T=	GRCh37
NC_000010.9:g.42935598T=	NCBI36
NG_007489.1:g.48076T= , LRG_518:g.48076T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2275T=	ENSP00000480088.2:p.Ser759=
ENST00000683007.1:n.2245T=
ENST00000683872.1:n.2236T=
ENST00000340058.6:c.2671T=	ENSP00000344798.4:p.Ser891=
ENST00000355710.8:c.2671T= MANE Select	ENSP00000347942.3:p.Ser891=
ENST00000671844.1:c.*1265T=	ENSP00000500541.1:n.*1265T=
ENST00000672389.1:c.*1265T=	ENSP00000500252.1:n.*1265T=
ENST00000340058.5:c.2671T=	ENSP00000344798.4:p.Ser891=
ENST00000355710.7:c.2671T=	ENSP00000347942.3:p.Ser891=
ENST00000615310.4:c.*20T=	ENSP00000480088.1:n.*20T=
NM_020630.4:c.2671T= , LRG_518t2:c.2671T=	NP_065681.1:p.Ser891=
NM_020975.4:c.2671T= , LRG_518t1:c.2671T=	NP_066124.1:p.Ser891=
XM_011540027.1:c.2671T=	XP_011538329.1:p.Ser891=
NM_001355216.1:c.1909T=	NP_001342145.1:p.Ser637=
NM_020630.5:c.2671T=	NP_065681.1:p.Ser891=
NM_020975.5:c.2671T=	NP_066124.1:p.Ser891=
NM_020975.6:c.2671T= MANE Select	NP_066124.1:p.Ser891=
NM_020630.6:c.2671T=	NP_065681.1:p.Ser891=