Canonical Allele Identifier: CA999404657
Gene: ALPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21563050_21563051insT , CM000663.2:g.21563050_21563051insT GRCh38
NC_000001.10:g.21889543_21889544insT , CM000663.1:g.21889543_21889544insT GRCh37
NC_000001.9:g.21762130_21762131insT NCBI36
NG_008940.1:g.58686_58687insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.298-60_298-59insT MANE Select ENSP00000363973.3:n.298-60_298-59insT
ENST00000374832.5:c.298-60_298-59insT ENSP00000363965.1:n.298-60_298-59insT
ENST00000374840.7:c.298-60_298-59insT ENSP00000363973.3:n.298-60_298-59insT
ENST00000468526.1:n.358-60_358-59insT
ENST00000539907.5:c.67-60_67-59insT ENSP00000437674.1:n.67-60_67-59insT
ENST00000540617.5:c.133-60_133-59insT ENSP00000442672.1:n.133-60_133-59insT
NM_000478.4:c.298-60_298-59insT NP_000469.3:n.298-60_298-59insT
NM_001127501.2:c.133-60_133-59insT NP_001120973.2:n.133-60_133-59insT
NM_001177520.1:c.67-60_67-59insT NP_001170991.1:n.67-60_67-59insT
XM_005245818.1:c.298-60_298-59insT XP_005245875.1:n.298-60_298-59insT
XM_005245820.2:c.298-60_298-59insT XP_005245877.1:n.298-60_298-59insT
XM_006710546.1:c.298-60_298-59insT XP_006710609.1:n.298-60_298-59insT
NM_000478.5:c.298-60_298-59insT NP_000469.3:n.298-60_298-59insT
NM_001127501.3:c.133-60_133-59insT NP_001120973.2:n.133-60_133-59insT
NM_001177520.2:c.67-60_67-59insT NP_001170991.1:n.67-60_67-59insT
XM_006710546.3:c.298-60_298-59insT XP_006710609.1:n.298-60_298-59insT
XM_017000903.1:c.142-60_142-59insT XP_016856392.1:n.142-60_142-59insT
NM_000478.6:c.298-60_298-59insT MANE Select NP_000469.3:n.298-60_298-59insT
NM_001127501.4:c.133-60_133-59insT NP_001120973.2:n.133-60_133-59insT
NM_001177520.3:c.67-60_67-59insT NP_001170991.1:n.67-60_67-59insT
NM_001369803.2:c.298-60_298-59insT NP_001356732.1:n.298-60_298-59insT
NM_001369804.2:c.298-60_298-59insT NP_001356733.1:n.298-60_298-59insT
NM_001369805.2:c.298-60_298-59insT NP_001356734.1:n.298-60_298-59insT