Canonical Allele Identifier: CA2643930001
Gene: ALPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21561068_21561071del , CM000663.2:g.21561068_21561071del GRCh38
NC_000001.10:g.21887561_21887564del , CM000663.1:g.21887561_21887564del GRCh37
NC_000001.9:g.21760148_21760151del NCBI36
NG_008940.1:g.56704_56707del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.182-29_182-26del MANE Select ENSP00000363973.3:n.182-29_182-26del
ENST00000374832.5:c.182-29_182-26del ENSP00000363965.1:n.182-29_182-26del
ENST00000374840.7:c.182-29_182-26del ENSP00000363973.3:n.182-29_182-26del
ENST00000468526.1:n.242-29_242-26del
ENST00000539907.5:c.66+323_66+326del ENSP00000437674.1:n.66+323_66+326del
ENST00000540617.5:c.17-29_17-26del ENSP00000442672.1:n.17-29_17-26del
NM_000478.4:c.182-29_182-26del NP_000469.3:n.182-29_182-26del
NM_001127501.2:c.17-29_17-26del NP_001120973.2:n.17-29_17-26del
NM_001177520.1:c.66+323_66+326del NP_001170991.1:n.66+323_66+326del
XM_005245818.1:c.182-29_182-26del XP_005245875.1:n.182-29_182-26del
XM_005245820.2:c.182-29_182-26del XP_005245877.1:n.182-29_182-26del
XM_006710546.1:c.182-29_182-26del XP_006710609.1:n.182-29_182-26del
NM_000478.5:c.182-29_182-26del NP_000469.3:n.182-29_182-26del
NM_001127501.3:c.17-29_17-26del NP_001120973.2:n.17-29_17-26del
NM_001177520.2:c.66+323_66+326del NP_001170991.1:n.66+323_66+326del
XM_006710546.3:c.182-29_182-26del XP_006710609.1:n.182-29_182-26del
XM_017000903.1:c.67-70_67-67del XP_016856392.1:n.67-70_67-67del
NM_000478.6:c.182-29_182-26del MANE Select NP_000469.3:n.182-29_182-26del
NM_001127501.4:c.17-29_17-26del NP_001120973.2:n.17-29_17-26del
NM_001177520.3:c.66+323_66+326del NP_001170991.1:n.66+323_66+326del
NM_001369803.2:c.182-29_182-26del NP_001356732.1:n.182-29_182-26del
NM_001369804.2:c.182-29_182-26del NP_001356733.1:n.182-29_182-26del
NM_001369805.2:c.182-29_182-26del NP_001356734.1:n.182-29_182-26del