Canonical Allele Identifier: CA658820988

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21568105delinsCTAA , CM000663.2:g.21568105delinsCTAA	GRCh38
NC_000001.10:g.21894598delinsCTAA , CM000663.1:g.21894598delinsCTAA	GRCh37
NC_000001.9:g.21767185delinsCTAA	NCBI36
NG_008940.1:g.63741delinsCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.650delinsCTAA MANE Select	ENSP00000363973.3:p.Val217delinsAlaLys
ENST00000374832.5:c.650delinsCTAA	ENSP00000363965.1:p.Val217delinsAlaLys
ENST00000374840.7:c.650delinsCTAA	ENSP00000363973.3:p.Val217delinsAlaLys
ENST00000539907.5:c.419delinsCTAA	ENSP00000437674.1:p.Val140delinsAlaLys
ENST00000540617.5:c.485delinsCTAA	ENSP00000442672.1:p.Val162delinsAlaLys
NM_000478.4:c.650delinsCTAA	NP_000469.3:p.Val217delinsAlaLys
NM_001127501.2:c.485delinsCTAA	NP_001120973.2:p.Val162delinsAlaLys
NM_001177520.1:c.419delinsCTAA	NP_001170991.1:p.Val140delinsAlaLys
XM_005245818.1:c.650delinsCTAA	XP_005245875.1:p.Val217delinsAlaLys
XM_005245820.2:c.650delinsCTAA	XP_005245877.1:p.Val217delinsAlaLys
XM_006710546.1:c.650delinsCTAA	XP_006710609.1:p.Val217delinsAlaLys
NM_000478.5:c.650delinsCTAA	NP_000469.3:p.Val217delinsAlaLys
NM_001127501.3:c.485delinsCTAA	NP_001120973.2:p.Val162delinsAlaLys
NM_001177520.2:c.419delinsCTAA	NP_001170991.1:p.Val140delinsAlaLys
XM_006710546.3:c.650delinsCTAA	XP_006710609.1:p.Val217delinsAlaLys
XM_017000903.1:c.494delinsCTAA	XP_016856392.1:p.Val165delinsAlaLys
NM_000478.6:c.650delinsCTAA MANE Select	NP_000469.3:p.Val217delinsAlaLys
NM_001127501.4:c.485delinsCTAA	NP_001120973.2:p.Val162delinsAlaLys
NM_001177520.3:c.419delinsCTAA	NP_001170991.1:p.Val140delinsAlaLys
NM_001369803.2:c.650delinsCTAA	NP_001356732.1:p.Val217delinsAlaLys
NM_001369804.2:c.650delinsCTAA	NP_001356733.1:p.Val217delinsAlaLys
NM_001369805.2:c.650delinsCTAA	NP_001356734.1:p.Val217delinsAlaLys