Canonical Allele Identifier: CA446211037

Gene: APC

Linked Data

• dbSNP Id: rs149347068
• gnomAD v4: 5-112843637-G-T
• MyVariant Identifiers: chr5:g.112179334G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843637G>T , CM000667.2:g.112843637G>T	GRCh38
NC_000005.9:g.112179334G>T , CM000667.1:g.112179334G>T	GRCh37
NC_000005.8:g.112207233G>T	NCBI36
NG_008481.4:g.156117G>T , LRG_130:g.156117G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.8097G>T	ENSP00000473355.2:p.Pro2699=
ENST00000505350.2:c.*8049G>T	ENSP00000481752.1:n.*8049G>T
ENST00000507379.6:c.7989G>T	ENSP00000423224.2:p.Pro2663=
ENST00000509732.6:c.8043G>T	ENSP00000426541.2:p.Pro2681=
ENST00000512211.7:c.8043G>T	ENSP00000423828.3:p.Pro2681=
ENST00000257430.9:c.8043G>T MANE Select	ENSP00000257430.4:p.Pro2681=
ENST00000257430.8:c.8043G>T	ENSP00000257430.4:p.Pro2681=
ENST00000508376.6:c.8043G>T	ENSP00000427089.2:p.Pro2681=
ENST00000520401.1:c.231-13012G>T
NM_000038.5:c.8043G>T	NP_000029.2:p.Pro2681=
NM_001127510.2:c.8043G>T	NP_001120982.1:p.Pro2681=
NM_001127511.2:c.7989G>T	NP_001120983.2:p.Pro2663=
NM_001354895.1:c.8043G>T	NP_001341824.1:p.Pro2681=
NM_001354896.1:c.8097G>T	NP_001341825.1:p.Pro2699=
NM_001354897.1:c.8073G>T	NP_001341826.1:p.Pro2691=
NM_001354898.1:c.7968G>T	NP_001341827.1:p.Pro2656=
NM_001354899.1:c.7959G>T	NP_001341828.1:p.Pro2653=
NM_001354900.1:c.7920G>T	NP_001341829.1:p.Pro2640=
NM_001354901.1:c.7866G>T	NP_001341830.1:p.Pro2622=
NM_001354902.1:c.7770G>T	NP_001341831.1:p.Pro2590=
NM_001354903.1:c.7740G>T	NP_001341832.1:p.Pro2580=
NM_001354904.1:c.7665G>T	NP_001341833.1:p.Pro2555=
NM_001354905.1:c.7563G>T	NP_001341834.1:p.Pro2521=
NM_001354906.1:c.7194G>T	NP_001341835.1:p.Pro2398=
NM_000038.6:c.8043G>T MANE Select	NP_000029.2:p.Pro2681=
NM_001127510.3:c.8043G>T	NP_001120982.1:p.Pro2681=
NM_001127511.3:c.7989G>T	NP_001120983.2:p.Pro2663=
NM_001354895.2:c.8043G>T	NP_001341824.1:p.Pro2681=
NM_001354896.2:c.8097G>T	NP_001341825.1:p.Pro2699=
NM_001354897.2:c.8073G>T	NP_001341826.1:p.Pro2691=
NM_001354898.2:c.7968G>T	NP_001341827.1:p.Pro2656=
NM_001354899.2:c.7959G>T	NP_001341828.1:p.Pro2653=
NM_001354900.2:c.7920G>T	NP_001341829.1:p.Pro2640=
NM_001354901.2:c.7866G>T	NP_001341830.1:p.Pro2622=
NM_001354902.2:c.7770G>T	NP_001341831.1:p.Pro2590=
NM_001354903.2:c.7740G>T	NP_001341832.1:p.Pro2580=
NM_001354904.2:c.7665G>T	NP_001341833.1:p.Pro2555=
NM_001354905.2:c.7563G>T	NP_001341834.1:p.Pro2521=
NM_001354906.2:c.7194G>T	NP_001341835.1:p.Pro2398=