Canonical Allele Identifier: CA2586966216

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21561103_21561120dup , CM000663.2:g.21561103_21561120dup	GRCh38
NC_000001.10:g.21887596_21887613dup , CM000663.1:g.21887596_21887613dup	GRCh37
NC_000001.9:g.21760183_21760200dup	NCBI36
NG_008940.1:g.56739_56756dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000374840.8:c.188_205dup MANE Select	ENSP00000363973.3:p.Thr68_Ala69insGlyValS...
ENST00000374832.5:c.188_205dup	ENSP00000363965.1:p.Thr68_Ala69insGlyValS...
ENST00000374840.7:c.188_205dup	ENSP00000363973.3:p.Thr68_Ala69insGlyValS...
ENST00000468526.1:n.248_265dup
ENST00000539907.5:c.66+358_66+375dup	ENSP00000437674.1:n.66+358_66+375dup
ENST00000540617.5:c.23_40dup	ENSP00000442672.1:p.Thr13_Ala14insGlyValS...
NM_000478.4:c.188_205dup	NP_000469.3:p.Thr68_Ala69insGlyValSerThrV...
NM_001127501.2:c.23_40dup	NP_001120973.2:p.Thr13_Ala14insGlyValSerT...
NM_001177520.1:c.66+358_66+375dup	NP_001170991.1:n.66+358_66+375dup
XM_005245818.1:c.188_205dup	XP_005245875.1:p.Thr68_Ala69insGlyValSerT...
XM_005245820.2:c.188_205dup	XP_005245877.1:p.Thr68_Ala69insGlyValSerT...
XM_006710546.1:c.188_205dup	XP_006710609.1:p.Thr68_Ala69insGlyValSerT...
NM_000478.5:c.188_205dup	NP_000469.3:p.Thr68_Ala69insGlyValSerThrV...
NM_001127501.3:c.23_40dup	NP_001120973.2:p.Thr13_Ala14insGlyValSerT...
NM_001177520.2:c.66+358_66+375dup	NP_001170991.1:n.66+358_66+375dup
XM_006710546.3:c.188_205dup	XP_006710609.1:p.Thr68_Ala69insGlyValSerT...
XM_017000903.1:c.67-35_67-18dup	XP_016856392.1:n.67-35_67-18dup
NM_000478.6:c.188_205dup MANE Select	NP_000469.3:p.Thr68_Ala69insGlyValSerThrV...
NM_001127501.4:c.23_40dup	NP_001120973.2:p.Thr13_Ala14insGlyValSerT...
NM_001177520.3:c.66+358_66+375dup	NP_001170991.1:n.66+358_66+375dup
NM_001369803.2:c.188_205dup	NP_001356732.1:p.Thr68_Ala69insGlyValSerT...
NM_001369804.2:c.188_205dup	NP_001356733.1:p.Thr68_Ala69insGlyValSerT...
NM_001369805.2:c.188_205dup	NP_001356734.1:p.Thr68_Ala69insGlyValSerT...