Canonical Allele Identifier: CA2695497926
Gene: ALPL HGNC NCBI

Linked Data

dbSNP Id: rs2148184854

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21573794_21573804dup , CM000663.2:g.21573794_21573804dup GRCh38
NC_000001.10:g.21900287_21900297dup , CM000663.1:g.21900287_21900297dup GRCh37
NC_000001.9:g.21772874_21772884dup NCBI36
NG_008940.1:g.69430_69440dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.992_997+5dup
ENST00000374830.2:c.73-1939_73-1929dup
ENST00000374832.5:c.992_997+5dup
ENST00000374840.7:c.992_997+5dup
ENST00000539907.5:c.761_766+5dup
ENST00000540617.5:c.827_832+5dup
NM_000478.4:c.992_997+5dup
NM_001127501.2:c.827_832+5dup
NM_001177520.1:c.761_766+5dup
XM_005245818.1:c.992_997+5dup
XM_005245820.2:c.992_997+5dup
XM_006710546.1:c.992_997+5dup
NM_000478.5:c.992_997+5dup
NM_001127501.3:c.827_832+5dup
NM_001177520.2:c.761_766+5dup
XM_006710546.3:c.992_997+5dup
XM_017000903.1:c.836_841+5dup
NM_000478.6:c.992_997+5dup
NM_001127501.4:c.827_832+5dup
NM_001177520.3:c.761_766+5dup
NM_001369803.2:c.992_997+5dup
NM_001369804.2:c.992_997+5dup
NM_001369805.2:c.992_997+5dup