Canonical Allele Identifier: CA2841555972
Gene: ALPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21576628dup , CM000663.2:g.21576628dup GRCh38
NC_000001.10:g.21903121dup , CM000663.1:g.21903121dup GRCh37
NC_000001.9:g.21775708dup NCBI36
NG_008940.1:g.72264dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.1296dup MANE Select ENSP00000363973.3:p.Met433HisfsTer?
ENST00000374829.2:n.565dup
ENST00000374830.2:c.371dup
ENST00000374832.5:c.1296dup ENSP00000363965.1:p.Met433HisfsTer?
ENST00000374840.7:c.1296dup ENSP00000363973.3:p.Met433HisfsTer?
ENST00000539907.5:c.1065dup ENSP00000437674.1:p.Met356HisfsTer?
ENST00000540617.5:c.1131dup ENSP00000442672.1:p.Met378HisfsTer?
NM_000478.4:c.1296dup NP_000469.3:p.Met433HisfsTer?
NM_001127501.2:c.1131dup NP_001120973.2:p.Met378HisfsTer?
NM_001177520.1:c.1065dup NP_001170991.1:p.Met356HisfsTer?
XM_005245818.1:c.1296dup XP_005245875.1:p.Met433HisfsTer?
XM_006710546.1:c.1296dup XP_006710609.1:p.Met433HisfsTer?
NM_000478.5:c.1296dup NP_000469.3:p.Met433HisfsTer?
NM_001127501.3:c.1131dup NP_001120973.2:p.Met378HisfsTer?
NM_001177520.2:c.1065dup NP_001170991.1:p.Met356HisfsTer?
XM_006710546.3:c.1296dup XP_006710609.1:p.Met433HisfsTer?
XM_017000903.1:c.1140dup XP_016856392.1:p.Met381HisfsTer?
NM_000478.6:c.1296dup MANE Select NP_000469.3:p.Met433HisfsTer?
NM_001127501.4:c.1131dup NP_001120973.2:p.Met378HisfsTer?
NM_001177520.3:c.1065dup NP_001170991.1:p.Met356HisfsTer?
NM_001369803.2:c.1296dup NP_001356732.1:p.Met433HisfsTer?
NM_001369804.2:c.1296dup NP_001356733.1:p.Met433HisfsTer?
NM_001369805.2:c.1296dup NP_001356734.1:p.Met433HisfsTer?