Canonical Allele Identifier: CA1905836919

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100778_43100805delinsCGCCCTTATCACAGCCGCTGACACTGAA , CM000672.2:g.43100778_43100805delinsCGCCCTTATCACAGCCGCTGACACTGAA	GRCh38
NC_000010.10:g.43596226_43596253delinsCGCCCTTATCACAGCCGCTGACACTGAA , CM000672.1:g.43596226_43596253delinsCGCCCTTATCACAGCCGCTGACACTGAA	GRCh37
NC_000010.9:g.42916232_42916259delinsCGCCCTTATCACAGCCGCTGACACTGAA	NCBI36
NG_007489.1:g.28710_28737delinsCGCCCTTATCACAGCCGCTGACACTGAA , LRG_518:g.28710_28737delinsCGCCCTTATCACAGCCGCTGACACTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	ENSP00000480088.2:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGAC...
ENST00000683278.1:c.239+56_239+83delinsCGCCCTTATCACAGCCGCTGACACTGAA
ENST00000684216.1:c.239+56_239+83delinsCGCCCTTATCACAGCCGCTGACACTGAA
ENST00000340058.6:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	ENSP00000344798.4:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGAC...
ENST00000355710.8:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA MANE Select	ENSP00000347942.3:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGAC...
ENST00000638465.1:c.239+56_239+83delinsCGCCCTTATCACAGCCGCTGACACTGAA
ENST00000640619.1:c.239+56_239+83delinsCGCCCTTATCACAGCCGCTGACACTGAA
ENST00000671844.1:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	ENSP00000500541.1:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGAC...
ENST00000672389.1:c.74-10429_74-10402delinsCGCCCTTATCACAGCCGCTGACACTGAA	ENSP00000500252.1:n.74-10429_74-10402delinsCGCCCTTATCACAGCCGC...
ENST00000340058.5:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	ENSP00000344798.4:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGAC...
ENST00000355710.7:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	ENSP00000347942.3:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGAC...
ENST00000498820.5:c.74-11321_74-11294delinsCGCCCTTATCACAGCCGCTGACACTGAA	ENSP00000419080.1:n.74-11321_74-11294delinsCGCCCTTATCACAGCCGC...
ENST00000615310.4:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	ENSP00000480088.1:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGAC...
NM_020630.4:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA , LRG_518t2:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	NP_065681.1:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA...
NM_020975.4:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA , LRG_518t1:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	NP_066124.1:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA...
XM_011540027.1:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	XP_011538329.1:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACT...
NM_020630.5:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	NP_065681.1:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA...
NM_020975.5:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	NP_066124.1:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA...
NM_020975.6:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA MANE Select	NP_066124.1:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA...
NM_020630.6:c.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA	NP_065681.1:n.337+56_337+83delinsCGCCCTTATCACAGCCGCTGACACTGAA...