Canonical Allele Identifier: CA239430371
Community Standard Title: NM_014515.7(CNOT2):c.1481A>G (p.Tyr494Cys)
Gene: CNOT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.70346269A>G , CM000674.2:g.70346269A>G GRCh38
NC_000012.11:g.70740049A>G , CM000674.1:g.70740049A>G GRCh37
NC_000012.10:g.69026316A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014515.7:c.1481A>G MANE Select NP_055330.1:p.Tyr494Cys
ENST00000229195.8:c.1481A>G MANE Select ENSP00000229195.3:p.Tyr494Cys
NM_001199302.1:c.1481A>G NP_001186231.1:p.Tyr494Cys
NM_001199302.2:c.1481A>G NP_001186231.1:p.Tyr494Cys
NM_001199303.1:c.1481A>G NP_001186232.1:p.Tyr494Cys
NM_001199303.2:c.1481A>G NP_001186232.1:p.Tyr494Cys
NM_014515.5:c.1481A>G NP_055330.1:p.Tyr494Cys
NM_014515.6:c.1481A>G NP_055330.1:p.Tyr494Cys
NR_037615.1:n.2409A>G
NR_037615.2:n.2382A>G
ENST00000229195.7:c.1481A>G ENSP00000229195.3:p.Tyr494Cys
ENST00000418359.7:c.1481A>G ENSP00000412091.3:p.Tyr494Cys
ENST00000546673.5:c.561A>G
ENST00000548159.5:c.1454A>G ENSP00000449659.1:p.Tyr485Cys
ENST00000548338.5:c.270+2041A>G
ENST00000549709.5:c.317A>G
ENST00000550641.6:c.1421A>G ENSP00000448024.2:p.Tyr474Cys
ENST00000550705.1:n.372A>G
ENST00000551043.5:c.1481A>G ENSP00000449260.1:p.Tyr494Cys
ENST00000551434.5:n.420A>G
ENST00000551483.5:c.434A>G ENSP00000448883.1:p.Tyr145Cys
ENST00000551710.1:c.230A>G ENSP00000447808.1:p.Tyr77Cys
XM_006719429.2:c.1454A>G XP_006719492.1:p.Tyr485Cys
XM_006719429.3:c.1454A>G XP_006719492.1:p.Tyr485Cys
XM_006719430.2:c.1454A>G XP_006719493.1:p.Tyr485Cys
XM_006719430.3:c.1454A>G XP_006719493.1:p.Tyr485Cys
XM_006719432.2:c.1298A>G XP_006719495.1:p.Tyr433Cys
XM_006719432.4:c.1298A>G XP_006719495.1:p.Tyr433Cys
XM_006719433.2:c.1070A>G XP_006719496.1:p.Tyr357Cys
XM_006719433.4:c.1070A>G XP_006719496.1:p.Tyr357Cys
XM_011538399.1:c.1481A>G XP_011536701.1:p.Tyr494Cys
XM_011538400.1:c.1421A>G XP_011536702.1:p.Tyr474Cys
XM_011538400.3:c.1421A>G XP_011536702.1:p.Tyr474Cys
XM_017019348.1:c.1454A>G XP_016874837.1:p.Tyr485Cys
XM_017019349.1:c.1454A>G XP_016874838.1:p.Tyr485Cys
XM_017019350.1:c.1421A>G XP_016874839.1:p.Tyr474Cys
XM_017019351.1:c.1421A>G XP_016874840.1:p.Tyr474Cys
XM_017019352.1:c.1421A>G XP_016874841.1:p.Tyr474Cys
XM_017019353.1:c.1043A>G XP_016874842.1:p.Tyr348Cys
XM_017019354.1:c.1043A>G XP_016874843.1:p.Tyr348Cys
XM_024448986.1:c.1043A>G XP_024304754.1:p.Tyr348Cys
XM_024448987.1:c.1010A>G XP_024304755.1:p.Tyr337Cys
XR_001748718.1:n.1854A>G