Canonical Allele Identifier: CA1158018323

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21573677_21573684delinsCAGGGGAC , CM000663.2:g.21573677_21573684delinsCAGGGGAC	GRCh38
NC_000001.10:g.21900170_21900177delinsCAGGGGAC , CM000663.1:g.21900170_21900177delinsCAGGGGAC	GRCh37
NC_000001.9:g.21772757_21772764delinsCAGGGGAC	NCBI36
NG_008940.1:g.69313_69320delinsCAGGGGAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000374840.8:c.875_882delinsCAGGGGAC MANE Select	ENSP00000363973.3:p.Pro292=
ENST00000374830.2:c.73-2056_73-2049delinsCAGGGGAC
ENST00000374832.5:c.875_882delinsCAGGGGAC	ENSP00000363965.1:p.Pro292=
ENST00000374840.7:c.875_882delinsCAGGGGAC	ENSP00000363973.3:p.Pro292=
ENST00000539907.5:c.644_651delinsCAGGGGAC	ENSP00000437674.1:p.Pro215=
ENST00000540617.5:c.710_717delinsCAGGGGAC	ENSP00000442672.1:p.Pro237=
NM_000478.4:c.875_882delinsCAGGGGAC	NP_000469.3:p.Pro292=
NM_001127501.2:c.710_717delinsCAGGGGAC	NP_001120973.2:p.Pro237=
NM_001177520.1:c.644_651delinsCAGGGGAC	NP_001170991.1:p.Pro215=
XM_005245818.1:c.875_882delinsCAGGGGAC	XP_005245875.1:p.Pro292=
XM_005245820.2:c.875_882delinsCAGGGGAC	XP_005245877.1:p.Pro292=
XM_006710546.1:c.875_882delinsCAGGGGAC	XP_006710609.1:p.Pro292=
NM_000478.5:c.875_882delinsCAGGGGAC	NP_000469.3:p.Pro292=
NM_001127501.3:c.710_717delinsCAGGGGAC	NP_001120973.2:p.Pro237=
NM_001177520.2:c.644_651delinsCAGGGGAC	NP_001170991.1:p.Pro215=
XM_006710546.3:c.875_882delinsCAGGGGAC	XP_006710609.1:p.Pro292=
XM_017000903.1:c.719_726delinsCAGGGGAC	XP_016856392.1:p.Pro240=
NM_000478.6:c.875_882delinsCAGGGGAC MANE Select	NP_000469.3:p.Pro292=
NM_001127501.4:c.710_717delinsCAGGGGAC	NP_001120973.2:p.Pro237=
NM_001177520.3:c.644_651delinsCAGGGGAC	NP_001170991.1:p.Pro215=
NM_001369803.2:c.875_882delinsCAGGGGAC	NP_001356732.1:p.Pro292=
NM_001369804.2:c.875_882delinsCAGGGGAC	NP_001356733.1:p.Pro292=
NM_001369805.2:c.875_882delinsCAGGGGAC	NP_001356734.1:p.Pro292=