Canonical Allele Identifier: CA1941444018
Gene: PLEKHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122432976A= , CM000672.2:g.122432976A= GRCh38
NC_000010.10:g.124192492A= , CM000672.1:g.124192492A= GRCh37
NC_000010.9:g.124182482A= NCBI36
NG_027823.1:g.63399A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368990.7:c.*3038A= ENSP00000357986.3:n.*3038A=
NM_001001974.3:c.*3038A= NP_001001974.1:n.*3038A=
NM_001195608.2:c.*3393A= NP_001182537.1:n.*3393A=
NM_001330178.2:c.*3142A= NP_001317107.1:n.*3142A=
NM_001377230.1:c.*3038A= NP_001364159.1:n.*3038A=
NM_001377231.1:c.*3038A= NP_001364160.1:n.*3038A=
NM_001377232.1:c.*3038A= NP_001364161.1:n.*3038A=
NM_001377234.1:c.*3038A= NP_001364163.1:n.*3038A=
NM_001377235.1:c.*3038A= NP_001364164.1:n.*3038A=
NM_001377237.1:c.*3393A= NP_001364166.1:n.*3393A=
NM_001377238.1:c.*3393A= NP_001364167.1:n.*3393A=
NM_001377240.1:c.*3142A= NP_001364169.1:n.*3142A=
NM_001377241.1:c.*3142A= NP_001364170.1:n.*3142A=
NM_001377242.1:c.*3142A= NP_001364171.1:n.*3142A=
NM_001377243.1:c.*3142A= NP_001364172.1:n.*3142A=
NM_001377244.1:c.*3142A= NP_001364173.1:n.*3142A=
NM_001377245.1:c.*3142A= NP_001364174.1:n.*3142A=
NM_001377246.1:c.*3142A= NP_001364175.1:n.*3142A=
NM_001377247.1:c.*3038A= NP_001364176.1:n.*3038A=
NM_001377248.1:c.*3142A= NP_001364177.1:n.*3142A=
NM_001377249.1:c.*3038A= NP_001364178.1:n.*3038A=
NM_001377250.1:c.*3142A= NP_001364179.1:n.*3142A=
NM_001377251.1:c.*3142A= NP_001364180.1:n.*3142A=
NM_001377252.1:c.*3038A= NP_001364181.1:n.*3038A=
NM_001377253.1:c.*3038A= NP_001364182.1:n.*3038A=
NM_001377254.1:c.*3038A= NP_001364183.1:n.*3038A=
NM_001377255.1:c.*3142A= NP_001364184.1:n.*3142A=
NM_001377256.1:c.*3142A= NP_001364185.1:n.*3142A=
NM_001377257.1:c.*3142A= NP_001364186.1:n.*3142A=
NM_001377258.1:c.*3385A= NP_001364187.1:n.*3385A=
NM_021622.5:c.*3038A= NP_067635.2:n.*3038A=
NR_165160.1:n.4531A=
NR_165161.1:n.4479A=
NR_165162.1:n.4344A=
NR_165164.1:n.4396A=
NR_165165.1:n.4490A=