Canonical Allele Identifier: CA338877960

Gene: ALPL

Linked Data

• ClinVar Variation Id: 1327158
• ClinVar RCV Id: RCV001787438
• dbSNP Id: rs199590449
• MyVariant Identifiers: chr1:g.21890603C>G (hg19) ; chr1:g.21564110C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21564110C>G , CM000663.2:g.21564110C>G	GRCh38
NC_000001.10:g.21890603C>G , CM000663.1:g.21890603C>G	GRCh37
NC_000001.9:g.21763190C>G	NCBI36
NG_008940.1:g.59746C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374840.8:c.542C>G MANE Select	ENSP00000363973.3:p.Ser181Trp
ENST00000374832.5:c.542C>G	ENSP00000363965.1:p.Ser181Trp
ENST00000374840.7:c.542C>G	ENSP00000363973.3:p.Ser181Trp
ENST00000468526.1:n.602C>G
ENST00000539907.5:c.311C>G	ENSP00000437674.1:p.Ser104Trp
ENST00000540617.5:c.377C>G	ENSP00000442672.1:p.Ser126Trp
NM_000478.4:c.542C>G	NP_000469.3:p.Ser181Trp
NM_001127501.2:c.377C>G	NP_001120973.2:p.Ser126Trp
NM_001177520.1:c.311C>G	NP_001170991.1:p.Ser104Trp
XM_005245818.1:c.542C>G	XP_005245875.1:p.Ser181Trp
XM_005245820.2:c.542C>G	XP_005245877.1:p.Ser181Trp
XM_006710546.1:c.542C>G	XP_006710609.1:p.Ser181Trp
NM_000478.5:c.542C>G	NP_000469.3:p.Ser181Trp
NM_001127501.3:c.377C>G	NP_001120973.2:p.Ser126Trp
NM_001177520.2:c.311C>G	NP_001170991.1:p.Ser104Trp
XM_006710546.3:c.542C>G	XP_006710609.1:p.Ser181Trp
XM_017000903.1:c.386C>G	XP_016856392.1:p.Ser129Trp
NM_000478.6:c.542C>G MANE Select	NP_000469.3:p.Ser181Trp
NM_001127501.4:c.377C>G	NP_001120973.2:p.Ser126Trp
NM_001177520.3:c.311C>G	NP_001170991.1:p.Ser104Trp
NM_001369803.2:c.542C>G	NP_001356732.1:p.Ser181Trp
NM_001369804.2:c.542C>G	NP_001356733.1:p.Ser181Trp
NM_001369805.2:c.542C>G	NP_001356734.1:p.Ser181Trp