Canonical Allele Identifier: CA1905813460

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114491G= , CM000672.2:g.43114491G=	GRCh38
NC_000010.10:g.43609939G= , CM000672.1:g.43609939G=	GRCh37
NC_000010.9:g.42929945G=	NCBI36
NG_007489.1:g.42423G= , LRG_518:g.42423G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1891G= MANE Select	NP_066124.1:p.Asp631=
ENST00000355710.8:c.1891G= MANE Select	ENSP00000347942.3:p.Asp631=
NM_001355216.1:c.1129G=	NP_001342145.1:p.Asp377=
NM_020630.4:c.1891G= , LRG_518t2:c.1891G=	NP_065681.1:p.Asp631=
NM_020630.5:c.1891G=	NP_065681.1:p.Asp631=
NM_020630.6:c.1891G=	NP_065681.1:p.Asp631=
NM_020975.4:c.1891G= , LRG_518t1:c.1891G=	NP_066124.1:p.Asp631=
NM_020975.5:c.1891G=	NP_066124.1:p.Asp631=
ENST00000340058.5:c.1891G=	ENSP00000344798.4:p.Asp631=
ENST00000340058.6:c.1891G=	ENSP00000344798.4:p.Asp631=
ENST00000355710.7:c.1891G=	ENSP00000347942.3:p.Asp631=
ENST00000498820.5:c.442G=	ENSP00000419080.1:p.Asp148=
ENST00000615310.4:c.1289+3259G=	ENSP00000480088.1:n.1289+3259G=
ENST00000615310.5:c.1495G=	ENSP00000480088.2:p.Asp499=
ENST00000671844.1:c.*485G=	ENSP00000500541.1:n.*485G=
ENST00000672389.1:c.*485G=	ENSP00000500252.1:n.*485G=
ENST00000683007.1:n.1465G=
ENST00000683872.1:n.1456G=
XM_011540027.1:c.1891G=	XP_011538329.1:p.Asp631=