Canonical Allele Identifier: CA1905817656

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118429C= , CM000672.2:g.43118429C=	GRCh38
NC_000010.10:g.43613877C= , CM000672.1:g.43613877C=	GRCh37
NC_000010.9:g.42933883C=	NCBI36
NG_007489.1:g.46361C= , LRG_518:g.46361C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1945C=	ENSP00000480088.2:p.Gln649=
ENST00000683007.1:n.1915C=
ENST00000683872.1:n.1906C=
ENST00000340058.6:c.2341C=	ENSP00000344798.4:p.Gln781=
ENST00000355710.8:c.2341C= MANE Select	ENSP00000347942.3:p.Gln781=
ENST00000671844.1:c.*935C=	ENSP00000500541.1:n.*935C=
ENST00000672389.1:c.*935C=	ENSP00000500252.1:n.*935C=
ENST00000340058.5:c.2341C=	ENSP00000344798.4:p.Gln781=
ENST00000355710.7:c.2341C=	ENSP00000347942.3:p.Gln781=
ENST00000615310.4:c.1290-1273C=	ENSP00000480088.1:n.1290-1273C=
NM_020630.4:c.2341C= , LRG_518t2:c.2341C=	NP_065681.1:p.Gln781=
NM_020975.4:c.2341C= , LRG_518t1:c.2341C=	NP_066124.1:p.Gln781=
XM_011540027.1:c.2341C=	XP_011538329.1:p.Gln781=
NM_001355216.1:c.1579C=	NP_001342145.1:p.Gln527=
NM_020630.5:c.2341C=	NP_065681.1:p.Gln781=
NM_020975.5:c.2341C=	NP_066124.1:p.Gln781=
NM_020975.6:c.2341C= MANE Select	NP_066124.1:p.Gln781=
NM_020630.6:c.2341C=	NP_065681.1:p.Gln781=