Canonical Allele Identifier: CA658832932

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.[43114501G>A;43119694C>G] , CM000672.2:g.[43114501G>A;43119694C>G]	GRCh38
NC_000010.10:g.[43609949G>A;43615142C>G] , CM000672.1:g.[43609949G>A;43615142C>G]	GRCh37
NC_000010.9:g.[42929955G>A;42935148C>G]	NCBI36
NG_007489.1:g.[42433G>A;47626C>G] , LRG_518:g.[42433G>A;47626C>G]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.[1505G>A;2160C>G]	ENSP00000480088.2:p.[Cys502Tyr;Ile720Met]
ENST00000683007.1:n.[1475G>A;2130C>G]
ENST00000683872.1:n.[1466G>A;2121C>G]
ENST00000340058.6:c.[1901G>A;2556C>G]	ENSP00000344798.4:p.[Cys634Tyr;Ile852Met]
ENST00000355710.8:c.[1901G>A;2556C>G] MANE Select	ENSP00000347942.3:p.[Cys634Tyr;Ile852Met]
ENST00000671844.1:c.[*495G>A;*1150C>G]	ENSP00000500541.1:n.[*495G>A;*1150C>G]
ENST00000672389.1:c.[*495G>A;*1150C>G]	ENSP00000500252.1:n.[*495G>A;*1150C>G]
ENST00000340058.5:c.[1901G>A;2556C>G]	ENSP00000344798.4:p.[Cys634Tyr;Ile852Met]
ENST00000355710.7:c.[1901G>A;2556C>G]	ENSP00000347942.3:p.[Cys634Tyr;Ile852Met]
ENST00000615310.4:c.[1289+3269G>A;1290-8C>G]	ENSP00000480088.1:n.[1289+3269G>A;1290-8C>G]
NM_020630.4:c.[1901G>A;2556C>G] , LRG_518t2:c.[1901G>A;2556C>G]	NP_065681.1:p.[Cys634Tyr;Ile852Met]
NM_020975.4:c.[1901G>A;2556C>G] , LRG_518t1:c.[1901G>A;2556C>G]	NP_066124.1:p.[Cys634Tyr;Ile852Met]
XM_011540027.1:c.[1901G>A;2556C>G]	XP_011538329.1:p.[Cys634Tyr;Ile852Met]
NM_001355216.1:c.[1139G>A;1794C>G]	NP_001342145.1:p.[Cys380Tyr;Ile598Met]
NM_020630.5:c.[1901G>A;2556C>G]	NP_065681.1:p.[Cys634Tyr;Ile852Met]
NM_020975.5:c.[1901G>A;2556C>G]	NP_066124.1:p.[Cys634Tyr;Ile852Met]
NM_020975.6:c.[1901G>A;2556C>G] MANE Select	NP_066124.1:p.[Cys634Tyr;Ile852Met]
NM_020630.6:c.[1901G>A;2556C>G]	NP_065681.1:p.[Cys634Tyr;Ile852Met]