Canonical Allele Identifier: CA16039118

Gene: APC

Linked Data

• dbSNP Id: rs2150000761
• MyVariant Identifiers: chr5:g.112179485G>T (hg19) ; chr5:g.112843788G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843788G>T , CM000667.2:g.112843788G>T	GRCh38
NC_000005.9:g.112179485G>T , CM000667.1:g.112179485G>T	GRCh37
NC_000005.8:g.112207384G>T	NCBI36
NG_008481.4:g.156268G>T , LRG_130:g.156268G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8248G>T	ENSP00000473355.2:p.Asp2750Tyr
ENST00000505350.2:c.*8200G>T	ENSP00000481752.1:n.*8200G>T
ENST00000507379.6:c.8140G>T	ENSP00000423224.2:p.Asp2714Tyr
ENST00000509732.6:c.8194G>T	ENSP00000426541.2:p.Asp2732Tyr
ENST00000512211.7:c.8194G>T	ENSP00000423828.3:p.Asp2732Tyr
ENST00000257430.9:c.8194G>T MANE Select	ENSP00000257430.4:p.Asp2732Tyr
ENST00000257430.8:c.8194G>T	ENSP00000257430.4:p.Asp2732Tyr
ENST00000508376.6:c.8194G>T	ENSP00000427089.2:p.Asp2732Tyr
ENST00000520401.1:c.231-12861G>T
NM_000038.5:c.8194G>T	NP_000029.2:p.Asp2732Tyr
NM_001127510.2:c.8194G>T	NP_001120982.1:p.Asp2732Tyr
NM_001127511.2:c.8140G>T	NP_001120983.2:p.Asp2714Tyr
NM_001354895.1:c.8194G>T	NP_001341824.1:p.Asp2732Tyr
NM_001354896.1:c.8248G>T	NP_001341825.1:p.Asp2750Tyr
NM_001354897.1:c.8224G>T	NP_001341826.1:p.Asp2742Tyr
NM_001354898.1:c.8119G>T	NP_001341827.1:p.Asp2707Tyr
NM_001354899.1:c.8110G>T	NP_001341828.1:p.Asp2704Tyr
NM_001354900.1:c.8071G>T	NP_001341829.1:p.Asp2691Tyr
NM_001354901.1:c.8017G>T	NP_001341830.1:p.Asp2673Tyr
NM_001354902.1:c.7921G>T	NP_001341831.1:p.Asp2641Tyr
NM_001354903.1:c.7891G>T	NP_001341832.1:p.Asp2631Tyr
NM_001354904.1:c.7816G>T	NP_001341833.1:p.Asp2606Tyr
NM_001354905.1:c.7714G>T	NP_001341834.1:p.Asp2572Tyr
NM_001354906.1:c.7345G>T	NP_001341835.1:p.Asp2449Tyr
NM_000038.6:c.8194G>T MANE Select	NP_000029.2:p.Asp2732Tyr
NM_001127510.3:c.8194G>T	NP_001120982.1:p.Asp2732Tyr
NM_001127511.3:c.8140G>T	NP_001120983.2:p.Asp2714Tyr
NM_001354895.2:c.8194G>T	NP_001341824.1:p.Asp2732Tyr
NM_001354896.2:c.8248G>T	NP_001341825.1:p.Asp2750Tyr
NM_001354897.2:c.8224G>T	NP_001341826.1:p.Asp2742Tyr
NM_001354898.2:c.8119G>T	NP_001341827.1:p.Asp2707Tyr
NM_001354899.2:c.8110G>T	NP_001341828.1:p.Asp2704Tyr
NM_001354900.2:c.8071G>T	NP_001341829.1:p.Asp2691Tyr
NM_001354901.2:c.8017G>T	NP_001341830.1:p.Asp2673Tyr
NM_001354902.2:c.7921G>T	NP_001341831.1:p.Asp2641Tyr
NM_001354903.2:c.7891G>T	NP_001341832.1:p.Asp2631Tyr
NM_001354904.2:c.7816G>T	NP_001341833.1:p.Asp2606Tyr
NM_001354905.2:c.7714G>T	NP_001341834.1:p.Asp2572Tyr
NM_001354906.2:c.7345G>T	NP_001341835.1:p.Asp2449Tyr