Canonical Allele Identifier: CA2572364558

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21560710dup , CM000663.2:g.21560710dup	GRCh38
NC_000001.10:g.21887203dup , CM000663.1:g.21887203dup	GRCh37
NC_000001.9:g.21759790dup	NCBI36
NG_008940.1:g.56346dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.146dup MANE Select	ENSP00000363973.3:p.Asn49LysfsTer4
ENST00000374832.5:c.146dup	ENSP00000363965.1:p.Asn49LysfsTer4
ENST00000374840.7:c.146dup	ENSP00000363973.3:p.Asn49LysfsTer4
ENST00000468526.1:n.206dup
ENST00000539907.5:c.31dup	ENSP00000437674.1:p.Thr11AsnfsTer22
ENST00000540617.5:c.-20dup	ENSP00000442672.1:n.-20dup
NM_000478.4:c.146dup	NP_000469.3:p.Asn49LysfsTer4
NM_001127501.2:c.-20dup	NP_001120973.2:n.-20dup
NM_001177520.1:c.31dup	NP_001170991.1:p.Thr11AsnfsTer22
XM_005245818.1:c.146dup	XP_005245875.1:p.Asn49LysfsTer4
XM_005245820.2:c.146dup	XP_005245877.1:p.Asn49LysfsTer4
XM_006710546.1:c.146dup	XP_006710609.1:p.Asn49LysfsTer4
NM_000478.5:c.146dup	NP_000469.3:p.Asn49LysfsTer4
NM_001127501.3:c.-20dup	NP_001120973.2:n.-20dup
NM_001177520.2:c.31dup	NP_001170991.1:p.Thr11AsnfsTer22
XM_006710546.3:c.146dup	XP_006710609.1:p.Asn49LysfsTer4
XM_017000903.1:c.31dup	XP_016856392.1:p.Thr11AsnfsTer?
NM_000478.6:c.146dup MANE Select	NP_000469.3:p.Asn49LysfsTer4
NM_001127501.4:c.-20dup	NP_001120973.2:n.-20dup
NM_001177520.3:c.31dup	NP_001170991.1:p.Thr11AsnfsTer22
NM_001369803.2:c.146dup	NP_001356732.1:p.Asn49LysfsTer4
NM_001369804.2:c.146dup	NP_001356733.1:p.Asn49LysfsTer4
NM_001369805.2:c.146dup	NP_001356734.1:p.Asn49LysfsTer4