Canonical Allele Identifier: CA1905828851

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43126673_43126674delinsTT , CM000672.2:g.43126673_43126674delinsTT	GRCh38
NC_000010.10:g.43622121_43622122delinsTT , CM000672.1:g.43622121_43622122delinsTT	GRCh37
NC_000010.9:g.42942127_42942128delinsTT	NCBI36
NG_007489.1:g.54605_54606delinsTT , LRG_518:g.54605_54606delinsTT

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.3138_3139delinsTT MANE Select	NP_066124.1:p.Pro1047Ser
ENST00000355710.8:c.3138_3139delinsTT MANE Select	ENSP00000347942.3:p.Pro1047Ser
NM_001355216.1:c.2376_2377delinsTT	NP_001342145.1:p.Pro793Ser
NM_020630.4:c.3138_3139delinsTT , LRG_518t2:c.3138_3139delinsTT	NP_065681.1:p.Pro1047Ser
NM_020630.5:c.3138_3139delinsTT	NP_065681.1:p.Pro1047Ser
NM_020630.6:c.3138_3139delinsTT	NP_065681.1:p.Pro1047Ser
NM_020975.4:c.3138_3139delinsTT , LRG_518t1:c.3138_3139delinsTT	NP_066124.1:p.Pro1047Ser
NM_020975.5:c.3138_3139delinsTT	NP_066124.1:p.Pro1047Ser
ENST00000340058.5:c.3138_3139delinsTT	ENSP00000344798.4:p.Pro1047Ser
ENST00000340058.6:c.3138_3139delinsTT	ENSP00000344798.4:p.Pro1047Ser
ENST00000355710.7:c.3138_3139delinsTT	ENSP00000347942.3:p.Pro1047Ser
ENST00000615310.4:c.*487_*488delinsTT	ENSP00000480088.1:n.*487_*488delinsTT
ENST00000615310.5:c.2742_2743delinsTT	ENSP00000480088.2:p.Pro915Ser
ENST00000671844.1:c.*1732_*1733delinsTT	ENSP00000500541.1:n.*1732_*1733delinsTT
ENST00000672389.1:c.*1732_*1733delinsTT	ENSP00000500252.1:n.*1732_*1733delinsTT
ENST00000683007.1:n.2712_2713delinsTT
XM_011540027.1:c.3138_3139delinsTT	XP_011538329.1:p.Pro1047Ser