Canonical Allele Identifier: CA2643931892
Gene: ALPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21576656_21576663del , CM000663.2:g.21576656_21576663del GRCh38
NC_000001.10:g.21903149_21903156del , CM000663.1:g.21903149_21903156del GRCh37
NC_000001.9:g.21775736_21775743del NCBI36
NG_008940.1:g.72292_72299del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.1309+15_1309+22del MANE Select ENSP00000363973.3:n.1309+15_1309+22del
ENST00000374829.2:n.578+15_578+22del
ENST00000374830.2:c.384+15_384+22del
ENST00000374832.5:c.1309+15_1309+22del ENSP00000363965.1:n.1309+15_1309+22del
ENST00000374840.7:c.1309+15_1309+22del ENSP00000363973.3:n.1309+15_1309+22del
ENST00000539907.5:c.1078+15_1078+22del ENSP00000437674.1:n.1078+15_1078+22del
ENST00000540617.5:c.1144+15_1144+22del ENSP00000442672.1:n.1144+15_1144+22del
NM_000478.4:c.1309+15_1309+22del NP_000469.3:n.1309+15_1309+22del
NM_001127501.2:c.1144+15_1144+22del NP_001120973.2:n.1144+15_1144+22del
NM_001177520.1:c.1078+15_1078+22del NP_001170991.1:n.1078+15_1078+22del
XM_005245818.1:c.1309+15_1309+22del XP_005245875.1:n.1309+15_1309+22del
XM_006710546.1:c.1309+15_1309+22del XP_006710609.1:n.1309+15_1309+22del
NM_000478.5:c.1309+15_1309+22del NP_000469.3:n.1309+15_1309+22del
NM_001127501.3:c.1144+15_1144+22del NP_001120973.2:n.1144+15_1144+22del
NM_001177520.2:c.1078+15_1078+22del NP_001170991.1:n.1078+15_1078+22del
XM_006710546.3:c.1309+15_1309+22del XP_006710609.1:n.1309+15_1309+22del
XM_017000903.1:c.1153+15_1153+22del XP_016856392.1:n.1153+15_1153+22del
NM_000478.6:c.1309+15_1309+22del MANE Select NP_000469.3:n.1309+15_1309+22del
NM_001127501.4:c.1144+15_1144+22del NP_001120973.2:n.1144+15_1144+22del
NM_001177520.3:c.1078+15_1078+22del NP_001170991.1:n.1078+15_1078+22del
NM_001369803.2:c.1309+15_1309+22del NP_001356732.1:n.1309+15_1309+22del
NM_001369804.2:c.1309+15_1309+22del NP_001356733.1:n.1309+15_1309+22del
NM_001369805.2:c.1309+15_1309+22del NP_001356734.1:n.1309+15_1309+22del