Canonical Allele Identifier: CA2574252797

Gene: ALPL

Linked Data

• gnomAD v4: 1-21570378-AGTGGAGGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21570388_21570396del , CM000663.2:g.21570388_21570396del	GRCh38
NC_000001.10:g.21896881_21896889del , CM000663.1:g.21896881_21896889del	GRCh37
NC_000001.9:g.21769468_21769476del	NCBI36
NG_008940.1:g.66024_66032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.862+14_862+22del MANE Select	ENSP00000363973.3:n.862+14_862+22del
ENST00000374830.2:c.72+14_72+22del
ENST00000374832.5:c.862+14_862+22del	ENSP00000363965.1:n.862+14_862+22del
ENST00000374840.7:c.862+14_862+22del	ENSP00000363973.3:n.862+14_862+22del
ENST00000539907.5:c.631+14_631+22del	ENSP00000437674.1:n.631+14_631+22del
ENST00000540617.5:c.697+14_697+22del	ENSP00000442672.1:n.697+14_697+22del
NM_000478.4:c.862+14_862+22del	NP_000469.3:n.862+14_862+22del
NM_001127501.2:c.697+14_697+22del	NP_001120973.2:n.697+14_697+22del
NM_001177520.1:c.631+14_631+22del	NP_001170991.1:n.631+14_631+22del
XM_005245818.1:c.862+14_862+22del	XP_005245875.1:n.862+14_862+22del
XM_005245820.2:c.862+14_862+22del	XP_005245877.1:n.862+14_862+22del
XM_006710546.1:c.862+14_862+22del	XP_006710609.1:n.862+14_862+22del
NM_000478.5:c.862+14_862+22del	NP_000469.3:n.862+14_862+22del
NM_001127501.3:c.697+14_697+22del	NP_001120973.2:n.697+14_697+22del
NM_001177520.2:c.631+14_631+22del	NP_001170991.1:n.631+14_631+22del
XM_006710546.3:c.862+14_862+22del	XP_006710609.1:n.862+14_862+22del
XM_017000903.1:c.706+14_706+22del	XP_016856392.1:n.706+14_706+22del
NM_000478.6:c.862+14_862+22del MANE Select	NP_000469.3:n.862+14_862+22del
NM_001127501.4:c.697+14_697+22del	NP_001120973.2:n.697+14_697+22del
NM_001177520.3:c.631+14_631+22del	NP_001170991.1:n.631+14_631+22del
NM_001369803.2:c.862+14_862+22del	NP_001356732.1:n.862+14_862+22del
NM_001369804.2:c.862+14_862+22del	NP_001356733.1:n.862+14_862+22del
NM_001369805.2:c.862+14_862+22del	NP_001356734.1:n.862+14_862+22del