Canonical Allele Identifier: CA338880272
Gene: ALPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21573715A>G , CM000663.2:g.21573715A>G GRCh38
NC_000001.10:g.21900208A>G , CM000663.1:g.21900208A>G GRCh37
NC_000001.9:g.21772795A>G NCBI36
NG_008940.1:g.69351A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.913A>G MANE Select ENSP00000363973.3:p.Thr305Ala
ENST00000374830.2:c.73-2018A>G
ENST00000374832.5:c.913A>G ENSP00000363965.1:p.Thr305Ala
ENST00000374840.7:c.913A>G ENSP00000363973.3:p.Thr305Ala
ENST00000539907.5:c.682A>G ENSP00000437674.1:p.Thr228Ala
ENST00000540617.5:c.748A>G ENSP00000442672.1:p.Thr250Ala
NM_000478.4:c.913A>G NP_000469.3:p.Thr305Ala
NM_001127501.2:c.748A>G NP_001120973.2:p.Thr250Ala
NM_001177520.1:c.682A>G NP_001170991.1:p.Thr228Ala
XM_005245818.1:c.913A>G XP_005245875.1:p.Thr305Ala
XM_005245820.2:c.913A>G XP_005245877.1:p.Thr305Ala
XM_006710546.1:c.913A>G XP_006710609.1:p.Thr305Ala
NM_000478.5:c.913A>G NP_000469.3:p.Thr305Ala
NM_001127501.3:c.748A>G NP_001120973.2:p.Thr250Ala
NM_001177520.2:c.682A>G NP_001170991.1:p.Thr228Ala
XM_006710546.3:c.913A>G XP_006710609.1:p.Thr305Ala
XM_017000903.1:c.757A>G XP_016856392.1:p.Thr253Ala
NM_000478.6:c.913A>G MANE Select NP_000469.3:p.Thr305Ala
NM_001127501.4:c.748A>G NP_001120973.2:p.Thr250Ala
NM_001177520.3:c.682A>G NP_001170991.1:p.Thr228Ala
NM_001369803.2:c.913A>G NP_001356732.1:p.Thr305Ala
NM_001369804.2:c.913A>G NP_001356733.1:p.Thr305Ala
NM_001369805.2:c.913A>G NP_001356734.1:p.Thr305Ala