Canonical Allele Identifier: CA2503094509
Gene: ALPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21563996_21563999del , CM000663.2:g.21563996_21563999del GRCh38
NC_000001.10:g.21890489_21890492del , CM000663.1:g.21890489_21890492del GRCh37
NC_000001.9:g.21763076_21763079del NCBI36
NG_008940.1:g.59632_59635del

Transcript Alleles

HGVS Amino-acid change
ENST00000374840.8:c.473-45_473-42del MANE Select ENSP00000363973.3:n.473-45_473-42del
ENST00000374832.5:c.473-45_473-42del ENSP00000363965.1:n.473-45_473-42del
ENST00000374840.7:c.473-45_473-42del ENSP00000363973.3:n.473-45_473-42del
ENST00000468526.1:n.533-45_533-42del
ENST00000539907.5:c.242-45_242-42del ENSP00000437674.1:n.242-45_242-42del
ENST00000540617.5:c.308-45_308-42del ENSP00000442672.1:n.308-45_308-42del
NM_000478.4:c.473-45_473-42del NP_000469.3:n.473-45_473-42del
NM_001127501.2:c.308-45_308-42del NP_001120973.2:n.308-45_308-42del
NM_001177520.1:c.242-45_242-42del NP_001170991.1:n.242-45_242-42del
XM_005245818.1:c.473-45_473-42del XP_005245875.1:n.473-45_473-42del
XM_005245820.2:c.473-45_473-42del XP_005245877.1:n.473-45_473-42del
XM_006710546.1:c.473-45_473-42del XP_006710609.1:n.473-45_473-42del
NM_000478.5:c.473-45_473-42del NP_000469.3:n.473-45_473-42del
NM_001127501.3:c.308-45_308-42del NP_001120973.2:n.308-45_308-42del
NM_001177520.2:c.242-45_242-42del NP_001170991.1:n.242-45_242-42del
XM_006710546.3:c.473-45_473-42del XP_006710609.1:n.473-45_473-42del
XM_017000903.1:c.317-45_317-42del XP_016856392.1:n.317-45_317-42del
NM_000478.6:c.473-45_473-42del MANE Select NP_000469.3:n.473-45_473-42del
NM_001127501.4:c.308-45_308-42del NP_001120973.2:n.308-45_308-42del
NM_001177520.3:c.242-45_242-42del NP_001170991.1:n.242-45_242-42del
NM_001369803.2:c.473-45_473-42del NP_001356732.1:n.473-45_473-42del
NM_001369804.2:c.473-45_473-42del NP_001356733.1:n.473-45_473-42del
NM_001369805.2:c.473-45_473-42del NP_001356734.1:n.473-45_473-42del