Canonical Allele Identifier: CA16031946
Community Standard Title: NM_000038.6(APC):c.4845C>G (p.Tyr1615Ter)
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840439C>G , CM000667.2:g.112840439C>G GRCh38
NC_000005.9:g.112176136C>G , CM000667.1:g.112176136C>G GRCh37
NC_000005.8:g.112204035C>G NCBI36
NG_008481.4:g.152919C>G , LRG_130:g.152919C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000038.6:c.4845C>G MANE Select NP_000029.2:p.Tyr1615Ter
ENST00000257430.9:c.4845C>G MANE Select ENSP00000257430.4:p.Tyr1615Ter
NM_000038.5:c.4845C>G NP_000029.2:p.Tyr1615Ter
NM_001127510.2:c.4845C>G NP_001120982.1:p.Tyr1615Ter
NM_001127510.3:c.4845C>G NP_001120982.1:p.Tyr1615Ter
NM_001127511.2:c.4791C>G NP_001120983.2:p.Tyr1597Ter
NM_001127511.3:c.4791C>G NP_001120983.2:p.Tyr1597Ter
NM_001354895.1:c.4845C>G NP_001341824.1:p.Tyr1615Ter
NM_001354895.2:c.4845C>G NP_001341824.1:p.Tyr1615Ter
NM_001354896.1:c.4899C>G NP_001341825.1:p.Tyr1633Ter
NM_001354896.2:c.4899C>G NP_001341825.1:p.Tyr1633Ter
NM_001354897.1:c.4875C>G NP_001341826.1:p.Tyr1625Ter
NM_001354897.2:c.4875C>G NP_001341826.1:p.Tyr1625Ter
NM_001354898.1:c.4770C>G NP_001341827.1:p.Tyr1590Ter
NM_001354898.2:c.4770C>G NP_001341827.1:p.Tyr1590Ter
NM_001354899.1:c.4761C>G NP_001341828.1:p.Tyr1587Ter
NM_001354899.2:c.4761C>G NP_001341828.1:p.Tyr1587Ter
NM_001354900.1:c.4722C>G NP_001341829.1:p.Tyr1574Ter
NM_001354900.2:c.4722C>G NP_001341829.1:p.Tyr1574Ter
NM_001354901.1:c.4668C>G NP_001341830.1:p.Tyr1556Ter
NM_001354901.2:c.4668C>G NP_001341830.1:p.Tyr1556Ter
NM_001354902.1:c.4572C>G NP_001341831.1:p.Tyr1524Ter
NM_001354902.2:c.4572C>G NP_001341831.1:p.Tyr1524Ter
NM_001354903.1:c.4542C>G NP_001341832.1:p.Tyr1514Ter
NM_001354903.2:c.4542C>G NP_001341832.1:p.Tyr1514Ter
NM_001354904.1:c.4467C>G NP_001341833.1:p.Tyr1489Ter
NM_001354904.2:c.4467C>G NP_001341833.1:p.Tyr1489Ter
NM_001354905.1:c.4365C>G NP_001341834.1:p.Tyr1455Ter
NM_001354905.2:c.4365C>G NP_001341834.1:p.Tyr1455Ter
NM_001354906.1:c.3996C>G NP_001341835.1:p.Tyr1332Ter
NM_001354906.2:c.3996C>G NP_001341835.1:p.Tyr1332Ter
ENST00000257430.8:c.4845C>G ENSP00000257430.4:p.Tyr1615Ter
ENST00000504915.3:c.4899C>G ENSP00000473355.2:p.Tyr1633Ter
ENST00000505350.2:c.*4851C>G ENSP00000481752.1:n.*4851C>G
ENST00000507379.6:c.4791C>G ENSP00000423224.2:p.Tyr1597Ter
ENST00000508376.6:c.4845C>G ENSP00000427089.2:p.Tyr1615Ter
ENST00000508624.5:c.*4167C>G ENSP00000424265.1:n.*4167C>G
ENST00000509732.6:c.4845C>G ENSP00000426541.2:p.Tyr1615Ter
ENST00000512211.7:c.4845C>G ENSP00000423828.3:p.Tyr1615Ter
ENST00000520401.1:c.230+11467C>G