Canonical Allele Identifier: CA1905819407

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119718G= , CM000672.2:g.43119718G=	GRCh38
NC_000010.10:g.43615166G= , CM000672.1:g.43615166G=	GRCh37
NC_000010.9:g.42935172G=	NCBI36
NG_007489.1:g.47650G= , LRG_518:g.47650G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2184G=	ENSP00000480088.2:p.Gln728=
ENST00000683007.1:n.2154G=
ENST00000683872.1:n.2145G=
ENST00000340058.6:c.2580G=	ENSP00000344798.4:p.Gln860=
ENST00000355710.8:c.2580G= MANE Select	ENSP00000347942.3:p.Gln860=
ENST00000671844.1:c.*1174G=	ENSP00000500541.1:n.*1174G=
ENST00000672389.1:c.*1174G=	ENSP00000500252.1:n.*1174G=
ENST00000340058.5:c.2580G=	ENSP00000344798.4:p.Gln860=
ENST00000355710.7:c.2580G=	ENSP00000347942.3:p.Gln860=
ENST00000615310.4:c.1306G=	ENSP00000480088.1:p.Gly436=
NM_020630.4:c.2580G= , LRG_518t2:c.2580G=	NP_065681.1:p.Gln860=
NM_020975.4:c.2580G= , LRG_518t1:c.2580G=	NP_066124.1:p.Gln860=
XM_011540027.1:c.2580G=	XP_011538329.1:p.Gln860=
NM_001355216.1:c.1818G=	NP_001342145.1:p.Gln606=
NM_020630.5:c.2580G=	NP_065681.1:p.Gln860=
NM_020975.5:c.2580G=	NP_066124.1:p.Gln860=
NM_020975.6:c.2580G= MANE Select	NP_066124.1:p.Gln860=
NM_020630.6:c.2580G=	NP_065681.1:p.Gln860=