Canonical Allele Identifier: CA2211961535
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389409_20389410delinsCA , CM000678.2:g.20389409_20389410delinsCA GRCh38
NC_000016.9:g.20400731_20400732delinsCA , CM000678.1:g.20400731_20400732delinsCA GRCh37
NC_000016.8:g.20308232_20308233delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302451.9:c.203-4559_203-4558delinsTG MANE Select ENSP00000305465.4:n.203-4559_203-4558delinsTG
ENST00000302451.8:c.203-4559_203-4558delinsTG ENSP00000305465.4:n.203-4559_203-4558delinsTG
ENST00000575561.1:c.203-501_203-500delinsTG ENSP00000459161.1:n.203-501_203-500delinsTG
NM_174924.1:c.203-4559_203-4558delinsTG NP_777584.1:n.203-4559_203-4558delinsTG
XM_006721024.1:c.203-4559_203-4558delinsTG XP_006721087.1:n.203-4559_203-4558delinsTG
XM_011545764.1:c.203-4559_203-4558delinsTG XP_011544066.1:n.203-4559_203-4558delinsTG
XM_011545765.1:c.203-4559_203-4558delinsTG XP_011544067.1:n.203-4559_203-4558delinsTG
XR_950754.1:n.457-4559_457-4558delinsTG
NM_174924.2:c.203-4559_203-4558delinsTG MANE Select NP_777584.1:n.203-4559_203-4558delinsTG