Canonical Allele Identifier: CA1905836799

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100561C= , CM000672.2:g.43100561C=	GRCh38
NC_000010.10:g.43596009C= , CM000672.1:g.43596009C=	GRCh37
NC_000010.9:g.42916015C=	NCBI36
NG_007489.1:g.28493C= , LRG_518:g.28493C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.176C=	ENSP00000480088.2:p.Ala59=
ENST00000683278.1:c.78C=
ENST00000684216.1:c.78C=
ENST00000340058.6:c.176C=	ENSP00000344798.4:p.Ala59=
ENST00000355710.8:c.176C= MANE Select	ENSP00000347942.3:p.Ala59=
ENST00000638465.1:c.78C=
ENST00000640619.1:c.78C=
ENST00000671844.1:c.176C=	ENSP00000500541.1:p.Ala59=
ENST00000672389.1:c.74-10646C=	ENSP00000500252.1:n.74-10646C=
ENST00000340058.5:c.176C=	ENSP00000344798.4:p.Ala59=
ENST00000355710.7:c.176C=	ENSP00000347942.3:p.Ala59=
ENST00000498820.5:c.74-11538C=	ENSP00000419080.1:n.74-11538C=
ENST00000615310.4:c.176C=	ENSP00000480088.1:p.Ala59=
NM_020630.4:c.176C= , LRG_518t2:c.176C=	NP_065681.1:p.Ala59=
NM_020975.4:c.176C= , LRG_518t1:c.176C=	NP_066124.1:p.Ala59=
XM_011540027.1:c.176C=	XP_011538329.1:p.Ala59=
NM_020630.5:c.176C=	NP_065681.1:p.Ala59=
NM_020975.5:c.176C=	NP_066124.1:p.Ala59=
NM_020975.6:c.176C= MANE Select	NP_066124.1:p.Ala59=
NM_020630.6:c.176C=	NP_065681.1:p.Ala59=