Canonical Allele Identifier: CA2643930962

Gene: ALPL

Linked Data

• gnomAD v4: 1-21573666-TCTCTTCGAGCCAGGGGACATG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21573668_21573688del , CM000663.2:g.21573668_21573688del	GRCh38
NC_000001.10:g.21900161_21900181del , CM000663.1:g.21900161_21900181del	GRCh37
NC_000001.9:g.21772748_21772768del	NCBI36
NG_008940.1:g.69304_69324del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.866_886del MANE Select	ENSP00000363973.3:p.Leu289_Met295del
ENST00000374830.2:c.73-2065_73-2045del
ENST00000374832.5:c.866_886del	ENSP00000363965.1:p.Leu289_Met295del
ENST00000374840.7:c.866_886del	ENSP00000363973.3:p.Leu289_Met295del
ENST00000539907.5:c.635_655del	ENSP00000437674.1:p.Leu212_Met218del
ENST00000540617.5:c.701_721del	ENSP00000442672.1:p.Leu234_Met240del
NM_000478.4:c.866_886del	NP_000469.3:p.Leu289_Met295del
NM_001127501.2:c.701_721del	NP_001120973.2:p.Leu234_Met240del
NM_001177520.1:c.635_655del	NP_001170991.1:p.Leu212_Met218del
XM_005245818.1:c.866_886del	XP_005245875.1:p.Leu289_Met295del
XM_005245820.2:c.866_886del	XP_005245877.1:p.Leu289_Met295del
XM_006710546.1:c.866_886del	XP_006710609.1:p.Leu289_Met295del
NM_000478.5:c.866_886del	NP_000469.3:p.Leu289_Met295del
NM_001127501.3:c.701_721del	NP_001120973.2:p.Leu234_Met240del
NM_001177520.2:c.635_655del	NP_001170991.1:p.Leu212_Met218del
XM_006710546.3:c.866_886del	XP_006710609.1:p.Leu289_Met295del
XM_017000903.1:c.710_730del	XP_016856392.1:p.Leu237_Met243del
NM_000478.6:c.866_886del MANE Select	NP_000469.3:p.Leu289_Met295del
NM_001127501.4:c.701_721del	NP_001120973.2:p.Leu234_Met240del
NM_001177520.3:c.635_655del	NP_001170991.1:p.Leu212_Met218del
NM_001369803.2:c.866_886del	NP_001356732.1:p.Leu289_Met295del
NM_001369804.2:c.866_886del	NP_001356733.1:p.Leu289_Met295del
NM_001369805.2:c.866_886del	NP_001356734.1:p.Leu289_Met295del