Canonical Allele Identifier: CA19067801

Gene: ALPL

Linked Data

• dbSNP Id: rs1042701600
• gnomAD v4: 1-21573565-G-T
• MyVariant Identifiers: chr1:g.21900058G>T (hg19) ; chr1:g.21573565G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21573565G>T , CM000663.2:g.21573565G>T	GRCh38
NC_000001.10:g.21900058G>T , CM000663.1:g.21900058G>T	GRCh37
NC_000001.9:g.21772645G>T	NCBI36
NG_008940.1:g.69201G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.863-100G>T MANE Select	ENSP00000363973.3:n.863-100G>T
ENST00000374830.2:c.73-2168G>T
ENST00000374832.5:c.863-100G>T	ENSP00000363965.1:n.863-100G>T
ENST00000374840.7:c.863-100G>T	ENSP00000363973.3:n.863-100G>T
ENST00000539907.5:c.632-100G>T	ENSP00000437674.1:n.632-100G>T
ENST00000540617.5:c.698-100G>T	ENSP00000442672.1:n.698-100G>T
NM_000478.4:c.863-100G>T	NP_000469.3:n.863-100G>T
NM_001127501.2:c.698-100G>T	NP_001120973.2:n.698-100G>T
NM_001177520.1:c.632-100G>T	NP_001170991.1:n.632-100G>T
XM_005245818.1:c.863-100G>T	XP_005245875.1:n.863-100G>T
XM_005245820.2:c.863-100G>T	XP_005245877.1:n.863-100G>T
XM_006710546.1:c.863-100G>T	XP_006710609.1:n.863-100G>T
NM_000478.5:c.863-100G>T	NP_000469.3:n.863-100G>T
NM_001127501.3:c.698-100G>T	NP_001120973.2:n.698-100G>T
NM_001177520.2:c.632-100G>T	NP_001170991.1:n.632-100G>T
XM_006710546.3:c.863-100G>T	XP_006710609.1:n.863-100G>T
XM_017000903.1:c.707-100G>T	XP_016856392.1:n.707-100G>T
NM_000478.6:c.863-100G>T MANE Select	NP_000469.3:n.863-100G>T
NM_001127501.4:c.698-100G>T	NP_001120973.2:n.698-100G>T
NM_001177520.3:c.632-100G>T	NP_001170991.1:n.632-100G>T
NM_001369803.2:c.863-100G>T	NP_001356732.1:n.863-100G>T
NM_001369804.2:c.863-100G>T	NP_001356733.1:n.863-100G>T
NM_001369805.2:c.863-100G>T	NP_001356734.1:n.863-100G>T