Canonical Allele Identifier: CA416530868

Gene: ALPL

Linked Data

• MyVariant Identifiers: chr1:g.21896803C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21570310C>G , CM000663.2:g.21570310C>G	GRCh38
NC_000001.10:g.21896803C>G , CM000663.1:g.21896803C>G	GRCh37
NC_000001.9:g.21769390C>G	NCBI36
NG_008940.1:g.65946C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.798C>G MANE Select	ENSP00000363973.3:p.Ser266=
ENST00000374830.2:c.8C>G
ENST00000374832.5:c.798C>G	ENSP00000363965.1:p.Ser266=
ENST00000374840.7:c.798C>G	ENSP00000363973.3:p.Ser266=
ENST00000539907.5:c.567C>G	ENSP00000437674.1:p.Ser189=
ENST00000540617.5:c.633C>G	ENSP00000442672.1:p.Ser211=
NM_000478.4:c.798C>G	NP_000469.3:p.Ser266=
NM_001127501.2:c.633C>G	NP_001120973.2:p.Ser211=
NM_001177520.1:c.567C>G	NP_001170991.1:p.Ser189=
XM_005245818.1:c.798C>G	XP_005245875.1:p.Ser266=
XM_005245820.2:c.798C>G	XP_005245877.1:p.Ser266=
XM_006710546.1:c.798C>G	XP_006710609.1:p.Ser266=
NM_000478.5:c.798C>G	NP_000469.3:p.Ser266=
NM_001127501.3:c.633C>G	NP_001120973.2:p.Ser211=
NM_001177520.2:c.567C>G	NP_001170991.1:p.Ser189=
XM_006710546.3:c.798C>G	XP_006710609.1:p.Ser266=
XM_017000903.1:c.642C>G	XP_016856392.1:p.Ser214=
NM_000478.6:c.798C>G MANE Select	NP_000469.3:p.Ser266=
NM_001127501.4:c.633C>G	NP_001120973.2:p.Ser211=
NM_001177520.3:c.567C>G	NP_001170991.1:p.Ser189=
NM_001369803.2:c.798C>G	NP_001356732.1:p.Ser266=
NM_001369804.2:c.798C>G	NP_001356733.1:p.Ser266=
NM_001369805.2:c.798C>G	NP_001356734.1:p.Ser266=