Canonical Allele Identifier: CA1905830292

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43128011G= , CM000672.2:g.43128011G=	GRCh38
NC_000010.10:g.43623459G= , CM000672.1:g.43623459G=	GRCh37
NC_000010.9:g.42943465G=	NCBI36
NG_007489.1:g.55943G= , LRG_518:g.55943G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.*1257G=	ENSP00000480088.2:n.*1257G=
ENST00000683007.1:n.4050G=
ENST00000355710.8:c.3188-101G= MANE Select	ENSP00000347942.3:n.3188-101G=
ENST00000355710.7:c.3188-101G=	ENSP00000347942.3:n.3188-101G=
ENST00000615310.4:c.*537-101G=	ENSP00000480088.1:n.*537-101G=
NM_020975.4:c.3188-101G= , LRG_518t1:c.3188-101G=	NP_066124.1:n.3188-101G=
XM_011540027.1:c.3188-101G=	XP_011538329.1:n.3188-101G=
NM_020975.5:c.3188-101G=	NP_066124.1:n.3188-101G=
NM_020975.6:c.3188-101G= MANE Select	NP_066124.1:n.3188-101G=