Canonical Allele Identifier: CA2643931146
Gene: ALPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21574087_21574096dup , CM000663.2:g.21574087_21574096dup GRCh38
NC_000001.10:g.21900580_21900589dup , CM000663.1:g.21900580_21900589dup GRCh37
NC_000001.9:g.21773167_21773176dup NCBI36
NG_008940.1:g.69723_69732dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.997+288_997+297dup MANE Select ENSP00000363973.3:n.997+288_997+297dup
ENST00000374830.2:c.73-1646_73-1637dup
ENST00000374832.5:c.997+288_997+297dup ENSP00000363965.1:n.997+288_997+297dup
ENST00000374840.7:c.997+288_997+297dup ENSP00000363973.3:n.997+288_997+297dup
ENST00000539907.5:c.766+288_766+297dup ENSP00000437674.1:n.766+288_766+297dup
ENST00000540617.5:c.832+288_832+297dup ENSP00000442672.1:n.832+288_832+297dup
NM_000478.4:c.997+288_997+297dup NP_000469.3:n.997+288_997+297dup
NM_001127501.2:c.832+288_832+297dup NP_001120973.2:n.832+288_832+297dup
NM_001177520.1:c.766+288_766+297dup NP_001170991.1:n.766+288_766+297dup
XM_005245818.1:c.997+288_997+297dup XP_005245875.1:n.997+288_997+297dup
XM_005245820.2:c.1043_1052dup XP_005245877.1:p.Ser352Ter
XM_006710546.1:c.997+288_997+297dup XP_006710609.1:n.997+288_997+297dup
NM_000478.5:c.997+288_997+297dup NP_000469.3:n.997+288_997+297dup
NM_001127501.3:c.832+288_832+297dup NP_001120973.2:n.832+288_832+297dup
NM_001177520.2:c.766+288_766+297dup NP_001170991.1:n.766+288_766+297dup
XM_006710546.3:c.997+288_997+297dup XP_006710609.1:n.997+288_997+297dup
XM_017000903.1:c.841+288_841+297dup XP_016856392.1:n.841+288_841+297dup
NM_000478.6:c.997+288_997+297dup MANE Select NP_000469.3:n.997+288_997+297dup
NM_001127501.4:c.832+288_832+297dup NP_001120973.2:n.832+288_832+297dup
NM_001177520.3:c.766+288_766+297dup NP_001170991.1:n.766+288_766+297dup
NM_001369803.2:c.997+288_997+297dup NP_001356732.1:n.997+288_997+297dup
NM_001369804.2:c.997+288_997+297dup NP_001356733.1:n.997+288_997+297dup
NM_001369805.2:c.997+288_997+297dup NP_001356734.1:n.997+288_997+297dup