Canonical Allele Identifier: CA338880345

Gene: ALPL

Linked Data

• ClinVar Variation Id: 960105
• ClinVar RCV Id: RCV001233568
• dbSNP Id: rs1644686464
• MyVariant Identifiers: chr1:g.21900244A>T (hg19) ; chr1:g.21573751A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21573751A>T , CM000663.2:g.21573751A>T	GRCh38
NC_000001.10:g.21900244A>T , CM000663.1:g.21900244A>T	GRCh37
NC_000001.9:g.21772831A>T	NCBI36
NG_008940.1:g.69387A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.949A>T MANE Select	ENSP00000363973.3:p.Ile317Phe
ENST00000374830.2:c.73-1982A>T
ENST00000374832.5:c.949A>T	ENSP00000363965.1:p.Ile317Phe
ENST00000374840.7:c.949A>T	ENSP00000363973.3:p.Ile317Phe
ENST00000539907.5:c.718A>T	ENSP00000437674.1:p.Ile240Phe
ENST00000540617.5:c.784A>T	ENSP00000442672.1:p.Ile262Phe
NM_000478.4:c.949A>T	NP_000469.3:p.Ile317Phe
NM_001127501.2:c.784A>T	NP_001120973.2:p.Ile262Phe
NM_001177520.1:c.718A>T	NP_001170991.1:p.Ile240Phe
XM_005245818.1:c.949A>T	XP_005245875.1:p.Ile317Phe
XM_005245820.2:c.949A>T	XP_005245877.1:p.Ile317Phe
XM_006710546.1:c.949A>T	XP_006710609.1:p.Ile317Phe
NM_000478.5:c.949A>T	NP_000469.3:p.Ile317Phe
NM_001127501.3:c.784A>T	NP_001120973.2:p.Ile262Phe
NM_001177520.2:c.718A>T	NP_001170991.1:p.Ile240Phe
XM_006710546.3:c.949A>T	XP_006710609.1:p.Ile317Phe
XM_017000903.1:c.793A>T	XP_016856392.1:p.Ile265Phe
NM_000478.6:c.949A>T MANE Select	NP_000469.3:p.Ile317Phe
NM_001127501.4:c.784A>T	NP_001120973.2:p.Ile262Phe
NM_001177520.3:c.718A>T	NP_001170991.1:p.Ile240Phe
NM_001369803.2:c.949A>T	NP_001356732.1:p.Ile317Phe
NM_001369804.2:c.949A>T	NP_001356733.1:p.Ile317Phe
NM_001369805.2:c.949A>T	NP_001356734.1:p.Ile317Phe