Canonical Allele Identifier: CA16032101

Gene: APC

Linked Data

• dbSNP Id: rs2149927256
• MyVariant Identifiers: chr5:g.112176206C>G (hg19) ; chr5:g.112840509C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840509C>G , CM000667.2:g.112840509C>G	GRCh38
NC_000005.9:g.112176206C>G , CM000667.1:g.112176206C>G	GRCh37
NC_000005.8:g.112204105C>G	NCBI36
NG_008481.4:g.152989C>G , LRG_130:g.152989C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4969C>G	ENSP00000473355.2:p.Pro1657Ala
ENST00000505350.2:c.*4921C>G	ENSP00000481752.1:n.*4921C>G
ENST00000507379.6:c.4861C>G	ENSP00000423224.2:p.Pro1621Ala
ENST00000509732.6:c.4915C>G	ENSP00000426541.2:p.Pro1639Ala
ENST00000512211.7:c.4915C>G	ENSP00000423828.3:p.Pro1639Ala
ENST00000257430.9:c.4915C>G MANE Select	ENSP00000257430.4:p.Pro1639Ala
ENST00000257430.8:c.4915C>G	ENSP00000257430.4:p.Pro1639Ala
ENST00000508376.6:c.4915C>G	ENSP00000427089.2:p.Pro1639Ala
ENST00000508624.5:c.*4237C>G	ENSP00000424265.1:n.*4237C>G
ENST00000520401.1:c.230+11537C>G
NM_000038.5:c.4915C>G	NP_000029.2:p.Pro1639Ala
NM_001127510.2:c.4915C>G	NP_001120982.1:p.Pro1639Ala
NM_001127511.2:c.4861C>G	NP_001120983.2:p.Pro1621Ala
NM_001354895.1:c.4915C>G	NP_001341824.1:p.Pro1639Ala
NM_001354896.1:c.4969C>G	NP_001341825.1:p.Pro1657Ala
NM_001354897.1:c.4945C>G	NP_001341826.1:p.Pro1649Ala
NM_001354898.1:c.4840C>G	NP_001341827.1:p.Pro1614Ala
NM_001354899.1:c.4831C>G	NP_001341828.1:p.Pro1611Ala
NM_001354900.1:c.4792C>G	NP_001341829.1:p.Pro1598Ala
NM_001354901.1:c.4738C>G	NP_001341830.1:p.Pro1580Ala
NM_001354902.1:c.4642C>G	NP_001341831.1:p.Pro1548Ala
NM_001354903.1:c.4612C>G	NP_001341832.1:p.Pro1538Ala
NM_001354904.1:c.4537C>G	NP_001341833.1:p.Pro1513Ala
NM_001354905.1:c.4435C>G	NP_001341834.1:p.Pro1479Ala
NM_001354906.1:c.4066C>G	NP_001341835.1:p.Pro1356Ala
NM_000038.6:c.4915C>G MANE Select	NP_000029.2:p.Pro1639Ala
NM_001127510.3:c.4915C>G	NP_001120982.1:p.Pro1639Ala
NM_001127511.3:c.4861C>G	NP_001120983.2:p.Pro1621Ala
NM_001354895.2:c.4915C>G	NP_001341824.1:p.Pro1639Ala
NM_001354896.2:c.4969C>G	NP_001341825.1:p.Pro1657Ala
NM_001354897.2:c.4945C>G	NP_001341826.1:p.Pro1649Ala
NM_001354898.2:c.4840C>G	NP_001341827.1:p.Pro1614Ala
NM_001354899.2:c.4831C>G	NP_001341828.1:p.Pro1611Ala
NM_001354900.2:c.4792C>G	NP_001341829.1:p.Pro1598Ala
NM_001354901.2:c.4738C>G	NP_001341830.1:p.Pro1580Ala
NM_001354902.2:c.4642C>G	NP_001341831.1:p.Pro1548Ala
NM_001354903.2:c.4612C>G	NP_001341832.1:p.Pro1538Ala
NM_001354904.2:c.4537C>G	NP_001341833.1:p.Pro1513Ala
NM_001354905.2:c.4435C>G	NP_001341834.1:p.Pro1479Ala
NM_001354906.2:c.4066C>G	NP_001341835.1:p.Pro1356Ala