Canonical Allele Identifier: CA469031357

Gene: RET

Linked Data

• MyVariant Identifiers: chr10:g.43620337C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43124889C>A , CM000672.2:g.43124889C>A	GRCh38
NC_000010.10:g.43620337C>A , CM000672.1:g.43620337C>A	GRCh37
NC_000010.9:g.42940343C>A	NCBI36
NG_007489.1:g.52821C>A , LRG_518:g.52821C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2550C>A	ENSP00000480088.2:p.Arg850=
ENST00000683007.1:n.2520C>A
ENST00000340058.6:c.2946C>A	ENSP00000344798.4:p.Arg982=
ENST00000355710.8:c.2946C>A MANE Select	ENSP00000347942.3:p.Arg982=
ENST00000671844.1:c.*1540C>A	ENSP00000500541.1:n.*1540C>A
ENST00000672389.1:c.*1540C>A	ENSP00000500252.1:n.*1540C>A
ENST00000340058.5:c.2946C>A	ENSP00000344798.4:p.Arg982=
ENST00000355710.7:c.2946C>A	ENSP00000347942.3:p.Arg982=
ENST00000615310.4:c.*295C>A	ENSP00000480088.1:n.*295C>A
NM_020630.4:c.2946C>A , LRG_518t2:c.2946C>A	NP_065681.1:p.Arg982=
NM_020975.4:c.2946C>A , LRG_518t1:c.2946C>A	NP_066124.1:p.Arg982=
XM_011540027.1:c.2946C>A	XP_011538329.1:p.Arg982=
NM_001355216.1:c.2184C>A	NP_001342145.1:p.Arg728=
NM_020630.5:c.2946C>A	NP_065681.1:p.Arg982=
NM_020975.5:c.2946C>A	NP_066124.1:p.Arg982=
NM_020975.6:c.2946C>A MANE Select	NP_066124.1:p.Arg982=
NM_020630.6:c.2946C>A	NP_065681.1:p.Arg982=