Canonical Allele Identifier: CA124962983

Gene: APC

Linked Data

• dbSNP Id: rs35881722
• gnomAD v2: 5-112146735-CAA-C
• gnomAD v3: 5-112811038-CAA-C
• gnomAD v4: 5-112811038-CAA-C
• MyVariant Identifiers: chr5:g.112146736_112146737del (hg19) ; chr5:g.112811039_112811040del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112811044_112811045del , CM000667.2:g.112811044_112811045del	GRCh38
NC_000005.9:g.112146741_112146742del , CM000667.1:g.112146741_112146742del	GRCh37
NC_000005.8:g.112174640_112174641del	NCBI36
NG_008481.4:g.123524_123525del , LRG_130:g.123524_123525del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.835-4451_835-4450del	ENSP00000484935.2:n.835-4451_835-4450del
ENST00000504915.3:c.835-4451_835-4450del	ENSP00000473355.2:n.835-4451_835-4450del
ENST00000505084.2:n.891-4451_891-4450del
ENST00000505350.2:c.*841-4451_*841-4450del	ENSP00000481752.1:n.*841-4451_*841-4450del
ENST00000507379.6:c.781-4451_781-4450del	ENSP00000423224.2:n.781-4451_781-4450del
ENST00000509732.6:c.835-4451_835-4450del	ENSP00000426541.2:n.835-4451_835-4450del
ENST00000512211.7:c.835-4451_835-4450del	ENSP00000423828.3:n.835-4451_835-4450del
ENST00000257430.9:c.835-4451_835-4450del MANE Select	ENSP00000257430.4:n.835-4451_835-4450del
ENST00000257430.8:c.835-4451_835-4450del	ENSP00000257430.4:n.835-4451_835-4450del
ENST00000507379.5:c.781-4451_781-4450del	ENSP00000423224.1:n.781-4451_781-4450del
ENST00000508376.6:c.835-4451_835-4450del	ENSP00000427089.2:n.835-4451_835-4450del
ENST00000508624.5:c.*156+733_*156+734del	ENSP00000424265.1:n.*156+733_*156+734del
ENST00000512211.6:c.835-4451_835-4450del	ENSP00000423828.2:n.835-4451_835-4450del
NM_000038.5:c.835-4451_835-4450del	NP_000029.2:n.835-4451_835-4450del
NM_001127510.2:c.835-4451_835-4450del	NP_001120982.1:n.835-4451_835-4450del
NM_001127511.2:c.781-4451_781-4450del	NP_001120983.2:n.781-4451_781-4450del
NM_001354895.1:c.835-4451_835-4450del	NP_001341824.1:n.835-4451_835-4450del
NM_001354896.1:c.835-4451_835-4450del	NP_001341825.1:n.835-4451_835-4450del
NM_001354897.1:c.865-4451_865-4450del	NP_001341826.1:n.865-4451_865-4450del
NM_001354898.1:c.760-4451_760-4450del	NP_001341827.1:n.760-4451_760-4450del
NM_001354899.1:c.751-4451_751-4450del	NP_001341828.1:n.751-4451_751-4450del
NM_001354900.1:c.658-4451_658-4450del	NP_001341829.1:n.658-4451_658-4450del
NM_001354901.1:c.658-4451_658-4450del	NP_001341830.1:n.658-4451_658-4450del
NM_001354902.1:c.865-4451_865-4450del	NP_001341831.1:n.865-4451_865-4450del
NM_001354903.1:c.835-4451_835-4450del	NP_001341832.1:n.835-4451_835-4450del
NM_001354904.1:c.760-4451_760-4450del	NP_001341833.1:n.760-4451_760-4450del
NM_001354905.1:c.658-4451_658-4450del	NP_001341834.1:n.658-4451_658-4450del
NM_001354906.1:c.-16+733_-16+734del	NP_001341835.1:n.-16+733_-16+734del
NM_000038.6:c.835-4451_835-4450del MANE Select	NP_000029.2:n.835-4451_835-4450del
NM_001127510.3:c.835-4451_835-4450del	NP_001120982.1:n.835-4451_835-4450del
NM_001127511.3:c.781-4451_781-4450del	NP_001120983.2:n.781-4451_781-4450del
NM_001354895.2:c.835-4451_835-4450del	NP_001341824.1:n.835-4451_835-4450del
NM_001354896.2:c.835-4451_835-4450del	NP_001341825.1:n.835-4451_835-4450del
NM_001354897.2:c.865-4451_865-4450del	NP_001341826.1:n.865-4451_865-4450del
NM_001354898.2:c.760-4451_760-4450del	NP_001341827.1:n.760-4451_760-4450del
NM_001354899.2:c.751-4451_751-4450del	NP_001341828.1:n.751-4451_751-4450del
NM_001354900.2:c.658-4451_658-4450del	NP_001341829.1:n.658-4451_658-4450del
NM_001354901.2:c.658-4451_658-4450del	NP_001341830.1:n.658-4451_658-4450del
NM_001354902.2:c.865-4451_865-4450del	NP_001341831.1:n.865-4451_865-4450del
NM_001354903.2:c.835-4451_835-4450del	NP_001341832.1:n.835-4451_835-4450del
NM_001354904.2:c.760-4451_760-4450del	NP_001341833.1:n.760-4451_760-4450del
NM_001354905.2:c.658-4451_658-4450del	NP_001341834.1:n.658-4451_658-4450del
NM_001354906.2:c.-16+733_-16+734del	NP_001341835.1:n.-16+733_-16+734del