Canonical Allele Identifier: CA2574252830

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21570432_21570433del , CM000663.2:g.21570432_21570433del	GRCh38
NC_000001.10:g.21896925_21896926del , CM000663.1:g.21896925_21896926del	GRCh37
NC_000001.9:g.21769512_21769513del	NCBI36
NG_008940.1:g.66068_66069del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.862+58_862+59del MANE Select	ENSP00000363973.3:n.862+58_862+59del
ENST00000374830.2:c.72+58_72+59del
ENST00000374832.5:c.862+58_862+59del	ENSP00000363965.1:n.862+58_862+59del
ENST00000374840.7:c.862+58_862+59del	ENSP00000363973.3:n.862+58_862+59del
ENST00000539907.5:c.631+58_631+59del	ENSP00000437674.1:n.631+58_631+59del
ENST00000540617.5:c.697+58_697+59del	ENSP00000442672.1:n.697+58_697+59del
NM_000478.4:c.862+58_862+59del	NP_000469.3:n.862+58_862+59del
NM_001127501.2:c.697+58_697+59del	NP_001120973.2:n.697+58_697+59del
NM_001177520.1:c.631+58_631+59del	NP_001170991.1:n.631+58_631+59del
XM_005245818.1:c.862+58_862+59del	XP_005245875.1:n.862+58_862+59del
XM_005245820.2:c.862+58_862+59del	XP_005245877.1:n.862+58_862+59del
XM_006710546.1:c.862+58_862+59del	XP_006710609.1:n.862+58_862+59del
NM_000478.5:c.862+58_862+59del	NP_000469.3:n.862+58_862+59del
NM_001127501.3:c.697+58_697+59del	NP_001120973.2:n.697+58_697+59del
NM_001177520.2:c.631+58_631+59del	NP_001170991.1:n.631+58_631+59del
XM_006710546.3:c.862+58_862+59del	XP_006710609.1:n.862+58_862+59del
XM_017000903.1:c.706+58_706+59del	XP_016856392.1:n.706+58_706+59del
NM_000478.6:c.862+58_862+59del MANE Select	NP_000469.3:n.862+58_862+59del
NM_001127501.4:c.697+58_697+59del	NP_001120973.2:n.697+58_697+59del
NM_001177520.3:c.631+58_631+59del	NP_001170991.1:n.631+58_631+59del
NM_001369803.2:c.862+58_862+59del	NP_001356732.1:n.862+58_862+59del
NM_001369804.2:c.862+58_862+59del	NP_001356733.1:n.862+58_862+59del
NM_001369805.2:c.862+58_862+59del	NP_001356734.1:n.862+58_862+59del