Canonical Allele Identifier: CA2674856429

Gene: APC

Linked Data

• gnomAD v4: 5-112828798-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828798A>G , CM000667.2:g.112828798A>G	GRCh38
NC_000005.9:g.112164495A>G , CM000667.1:g.112164495A>G	GRCh37
NC_000005.8:g.112192394A>G	NCBI36
NG_008481.4:g.141278A>G , LRG_130:g.141278A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1409-6153A>G	ENSP00000484935.2:n.1409-6153A>G
ENST00000504915.3:c.1681-58A>G	ENSP00000473355.2:n.1681-58A>G
ENST00000505084.2:n.1683-58A>G
ENST00000505350.2:c.*1633-58A>G	ENSP00000481752.1:n.*1633-58A>G
ENST00000507379.6:c.1573-58A>G	ENSP00000423224.2:n.1573-58A>G
ENST00000509732.6:c.1627-58A>G	ENSP00000426541.2:n.1627-58A>G
ENST00000512211.7:c.1627-58A>G	ENSP00000423828.3:n.1627-58A>G
ENST00000257430.9:c.1627-58A>G MANE Select	ENSP00000257430.4:n.1627-58A>G
ENST00000257430.8:c.1627-58A>G	ENSP00000257430.4:n.1627-58A>G
ENST00000502371.2:c.97-6153A>G
ENST00000504915.2:c.316-58A>G	ENSP00000473355.1:n.316-58A>G
ENST00000505084.1:n.114-58A>G
ENST00000507379.5:c.1573-58A>G	ENSP00000423224.1:n.1573-58A>G
ENST00000508376.6:c.1627-58A>G	ENSP00000427089.2:n.1627-58A>G
ENST00000508624.5:c.*949-58A>G	ENSP00000424265.1:n.*949-58A>G
ENST00000512211.6:c.1627-58A>G	ENSP00000423828.2:n.1627-58A>G
ENST00000520401.1:c.114-58A>G
NM_000038.5:c.1627-58A>G	NP_000029.2:n.1627-58A>G
NM_001127510.2:c.1627-58A>G	NP_001120982.1:n.1627-58A>G
NM_001127511.2:c.1573-58A>G	NP_001120983.2:n.1573-58A>G
NM_001354895.1:c.1627-58A>G	NP_001341824.1:n.1627-58A>G
NM_001354896.1:c.1681-58A>G	NP_001341825.1:n.1681-58A>G
NM_001354897.1:c.1657-58A>G	NP_001341826.1:n.1657-58A>G
NM_001354898.1:c.1552-58A>G	NP_001341827.1:n.1552-58A>G
NM_001354899.1:c.1543-58A>G	NP_001341828.1:n.1543-58A>G
NM_001354900.1:c.1504-58A>G	NP_001341829.1:n.1504-58A>G
NM_001354901.1:c.1450-58A>G	NP_001341830.1:n.1450-58A>G
NM_001354902.1:c.1354-58A>G	NP_001341831.1:n.1354-58A>G
NM_001354903.1:c.1324-58A>G	NP_001341832.1:n.1324-58A>G
NM_001354904.1:c.1249-58A>G	NP_001341833.1:n.1249-58A>G
NM_001354905.1:c.1147-58A>G	NP_001341834.1:n.1147-58A>G
NM_001354906.1:c.778-58A>G	NP_001341835.1:n.778-58A>G
NM_000038.6:c.1627-58A>G MANE Select	NP_000029.2:n.1627-58A>G
NM_001127510.3:c.1627-58A>G	NP_001120982.1:n.1627-58A>G
NM_001127511.3:c.1573-58A>G	NP_001120983.2:n.1573-58A>G
NM_001354895.2:c.1627-58A>G	NP_001341824.1:n.1627-58A>G
NM_001354896.2:c.1681-58A>G	NP_001341825.1:n.1681-58A>G
NM_001354897.2:c.1657-58A>G	NP_001341826.1:n.1657-58A>G
NM_001354898.2:c.1552-58A>G	NP_001341827.1:n.1552-58A>G
NM_001354899.2:c.1543-58A>G	NP_001341828.1:n.1543-58A>G
NM_001354900.2:c.1504-58A>G	NP_001341829.1:n.1504-58A>G
NM_001354901.2:c.1450-58A>G	NP_001341830.1:n.1450-58A>G
NM_001354902.2:c.1354-58A>G	NP_001341831.1:n.1354-58A>G
NM_001354903.2:c.1324-58A>G	NP_001341832.1:n.1324-58A>G
NM_001354904.2:c.1249-58A>G	NP_001341833.1:n.1249-58A>G
NM_001354905.2:c.1147-58A>G	NP_001341834.1:n.1147-58A>G
NM_001354906.2:c.778-58A>G	NP_001341835.1:n.778-58A>G