Canonical Allele Identifier: CA2611240235
Gene: PLEKHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122432926G>T , CM000672.2:g.122432926G>T GRCh38
NC_000010.10:g.124192442G>T , CM000672.1:g.124192442G>T GRCh37
NC_000010.9:g.124182432G>T NCBI36
NG_027823.1:g.63349G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368990.7:c.*2988G>T ENSP00000357986.3:n.*2988G>T
NM_001001974.3:c.*2988G>T NP_001001974.1:n.*2988G>T
NM_001195608.2:c.*3343G>T NP_001182537.1:n.*3343G>T
NM_001330178.2:c.*3092G>T NP_001317107.1:n.*3092G>T
NM_001377230.1:c.*2988G>T NP_001364159.1:n.*2988G>T
NM_001377231.1:c.*2988G>T NP_001364160.1:n.*2988G>T
NM_001377232.1:c.*2988G>T NP_001364161.1:n.*2988G>T
NM_001377234.1:c.*2988G>T NP_001364163.1:n.*2988G>T
NM_001377235.1:c.*2988G>T NP_001364164.1:n.*2988G>T
NM_001377237.1:c.*3343G>T NP_001364166.1:n.*3343G>T
NM_001377238.1:c.*3343G>T NP_001364167.1:n.*3343G>T
NM_001377240.1:c.*3092G>T NP_001364169.1:n.*3092G>T
NM_001377241.1:c.*3092G>T NP_001364170.1:n.*3092G>T
NM_001377242.1:c.*3092G>T NP_001364171.1:n.*3092G>T
NM_001377243.1:c.*3092G>T NP_001364172.1:n.*3092G>T
NM_001377244.1:c.*3092G>T NP_001364173.1:n.*3092G>T
NM_001377245.1:c.*3092G>T NP_001364174.1:n.*3092G>T
NM_001377246.1:c.*3092G>T NP_001364175.1:n.*3092G>T
NM_001377247.1:c.*2988G>T NP_001364176.1:n.*2988G>T
NM_001377248.1:c.*3092G>T NP_001364177.1:n.*3092G>T
NM_001377249.1:c.*2988G>T NP_001364178.1:n.*2988G>T
NM_001377250.1:c.*3092G>T NP_001364179.1:n.*3092G>T
NM_001377251.1:c.*3092G>T NP_001364180.1:n.*3092G>T
NM_001377252.1:c.*2988G>T NP_001364181.1:n.*2988G>T
NM_001377253.1:c.*2988G>T NP_001364182.1:n.*2988G>T
NM_001377254.1:c.*2988G>T NP_001364183.1:n.*2988G>T
NM_001377255.1:c.*3092G>T NP_001364184.1:n.*3092G>T
NM_001377256.1:c.*3092G>T NP_001364185.1:n.*3092G>T
NM_001377257.1:c.*3092G>T NP_001364186.1:n.*3092G>T
NM_001377258.1:c.*3335G>T NP_001364187.1:n.*3335G>T
NM_021622.5:c.*2988G>T NP_067635.2:n.*2988G>T
NR_165160.1:n.4481G>T
NR_165161.1:n.4429G>T
NR_165162.1:n.4294G>T
NR_165164.1:n.4346G>T
NR_165165.1:n.4440G>T