Canonical Allele Identifier: CA1905828741

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43126647A= , CM000672.2:g.43126647A=	GRCh38
NC_000010.10:g.43622095A= , CM000672.1:g.43622095A=	GRCh37
NC_000010.9:g.42942101A=	NCBI36
NG_007489.1:g.54579A= , LRG_518:g.54579A=

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.3112A= MANE Select	NP_066124.1:p.Thr1038=
ENST00000355710.8:c.3112A= MANE Select	ENSP00000347942.3:p.Thr1038=
NM_001355216.1:c.2350A=	NP_001342145.1:p.Thr784=
NM_020630.4:c.3112A= , LRG_518t2:c.3112A=	NP_065681.1:p.Thr1038=
NM_020630.5:c.3112A=	NP_065681.1:p.Thr1038=
NM_020630.6:c.3112A=	NP_065681.1:p.Thr1038=
NM_020975.4:c.3112A= , LRG_518t1:c.3112A=	NP_066124.1:p.Thr1038=
NM_020975.5:c.3112A=	NP_066124.1:p.Thr1038=
ENST00000340058.5:c.3112A=	ENSP00000344798.4:p.Thr1038=
ENST00000340058.6:c.3112A=	ENSP00000344798.4:p.Thr1038=
ENST00000355710.7:c.3112A=	ENSP00000347942.3:p.Thr1038=
ENST00000615310.4:c.*461A=	ENSP00000480088.1:n.*461A=
ENST00000615310.5:c.2716A=	ENSP00000480088.2:p.Thr906=
ENST00000671844.1:c.*1706A=	ENSP00000500541.1:n.*1706A=
ENST00000672389.1:c.*1706A=	ENSP00000500252.1:n.*1706A=
ENST00000683007.1:n.2686A=
XM_011540027.1:c.3112A=	XP_011538329.1:p.Thr1038=