Canonical Allele Identifier: CA2608894444

Gene: RET

Linked Data

• gnomAD v4: 10-43100749-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100749_43100750insA , CM000672.2:g.43100749_43100750insA	GRCh38
NC_000010.10:g.43596197_43596198insA , CM000672.1:g.43596197_43596198insA	GRCh37
NC_000010.9:g.42916203_42916204insA	NCBI36
NG_007489.1:g.28681_28682insA , LRG_518:g.28681_28682insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+27_337+28insA	ENSP00000480088.2:n.337+27_337+28insA
ENST00000683278.1:c.239+27_239+28insA
ENST00000684216.1:c.239+27_239+28insA
ENST00000340058.6:c.337+27_337+28insA	ENSP00000344798.4:n.337+27_337+28insA
ENST00000355710.8:c.337+27_337+28insA MANE Select	ENSP00000347942.3:n.337+27_337+28insA
ENST00000638465.1:c.239+27_239+28insA
ENST00000640619.1:c.239+27_239+28insA
ENST00000671844.1:c.337+27_337+28insA	ENSP00000500541.1:n.337+27_337+28insA
ENST00000672389.1:c.74-10458_74-10457insA	ENSP00000500252.1:n.74-10458_74-10457insA
ENST00000340058.5:c.337+27_337+28insA	ENSP00000344798.4:n.337+27_337+28insA
ENST00000355710.7:c.337+27_337+28insA	ENSP00000347942.3:n.337+27_337+28insA
ENST00000498820.5:c.74-11350_74-11349insA	ENSP00000419080.1:n.74-11350_74-11349insA
ENST00000615310.4:c.337+27_337+28insA	ENSP00000480088.1:n.337+27_337+28insA
NM_020630.4:c.337+27_337+28insA , LRG_518t2:c.337+27_337+28insA	NP_065681.1:n.337+27_337+28insA
NM_020975.4:c.337+27_337+28insA , LRG_518t1:c.337+27_337+28insA	NP_066124.1:n.337+27_337+28insA
XM_011540027.1:c.337+27_337+28insA	XP_011538329.1:n.337+27_337+28insA
NM_020630.5:c.337+27_337+28insA	NP_065681.1:n.337+27_337+28insA
NM_020975.5:c.337+27_337+28insA	NP_066124.1:n.337+27_337+28insA
NM_020975.6:c.337+27_337+28insA MANE Select	NP_066124.1:n.337+27_337+28insA
NM_020630.6:c.337+27_337+28insA	NP_065681.1:n.337+27_337+28insA