Canonical Allele Identifier: CA2721856954
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs2132665766

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100727_43100728insCATCCCT , CM000672.2:g.43100727_43100728insCATCCCT GRCh38
NC_000010.10:g.43596175_43596176insCATCCCT , CM000672.1:g.43596175_43596176insCATCCCT GRCh37
NC_000010.9:g.42916181_42916182insCATCCCT NCBI36
NG_007489.1:g.28659_28660insCATCCCT , LRG_518:g.28659_28660insCATCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.337+5_337+6insCATCCCT ENSP00000480088.2:n.337+5_337+6insCATCCCT
ENST00000683278.1:c.239+5_239+6insCATCCCT
ENST00000684216.1:c.239+5_239+6insCATCCCT
ENST00000340058.6:c.337+5_337+6insCATCCCT ENSP00000344798.4:n.337+5_337+6insCATCCCT
ENST00000355710.8:c.337+5_337+6insCATCCCT MANE Select ENSP00000347942.3:n.337+5_337+6insCATCCCT
ENST00000638465.1:c.239+5_239+6insCATCCCT
ENST00000640619.1:c.239+5_239+6insCATCCCT
ENST00000671844.1:c.337+5_337+6insCATCCCT ENSP00000500541.1:n.337+5_337+6insCATCCCT
ENST00000672389.1:c.74-10480_74-10479insCATCCCT ENSP00000500252.1:n.74-10480_74-10479insCATCCCT
ENST00000340058.5:c.337+5_337+6insCATCCCT ENSP00000344798.4:n.337+5_337+6insCATCCCT
ENST00000355710.7:c.337+5_337+6insCATCCCT ENSP00000347942.3:n.337+5_337+6insCATCCCT
ENST00000498820.5:c.74-11372_74-11371insCATCCCT ENSP00000419080.1:n.74-11372_74-11371insCATCCCT
ENST00000615310.4:c.337+5_337+6insCATCCCT ENSP00000480088.1:n.337+5_337+6insCATCCCT
NM_020630.4:c.337+5_337+6insCATCCCT , LRG_518t2:c.337+5_337+6insCATCCCT NP_065681.1:n.337+5_337+6insCATCCCT
NM_020975.4:c.337+5_337+6insCATCCCT , LRG_518t1:c.337+5_337+6insCATCCCT NP_066124.1:n.337+5_337+6insCATCCCT
XM_011540027.1:c.337+5_337+6insCATCCCT XP_011538329.1:n.337+5_337+6insCATCCCT
NM_020630.5:c.337+5_337+6insCATCCCT NP_065681.1:n.337+5_337+6insCATCCCT
NM_020975.5:c.337+5_337+6insCATCCCT NP_066124.1:n.337+5_337+6insCATCCCT
NM_020975.6:c.337+5_337+6insCATCCCT MANE Select NP_066124.1:n.337+5_337+6insCATCCCT
NM_020630.6:c.337+5_337+6insCATCCCT NP_065681.1:n.337+5_337+6insCATCCCT