Canonical Allele Identifier: CA2211961515
Gene: PDILT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389353_20389354delinsTC , CM000678.2:g.20389353_20389354delinsTC GRCh38
NC_000016.9:g.20400675_20400676delinsTC , CM000678.1:g.20400675_20400676delinsTC GRCh37
NC_000016.8:g.20308176_20308177delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302451.9:c.203-4503_203-4502delinsGA MANE Select ENSP00000305465.4:n.203-4503_203-4502delinsGA
ENST00000302451.8:c.203-4503_203-4502delinsGA ENSP00000305465.4:n.203-4503_203-4502delinsGA
ENST00000575561.1:c.203-445_203-444delinsGA ENSP00000459161.1:n.203-445_203-444delinsGA
NM_174924.1:c.203-4503_203-4502delinsGA NP_777584.1:n.203-4503_203-4502delinsGA
XM_006721024.1:c.203-4503_203-4502delinsGA XP_006721087.1:n.203-4503_203-4502delinsGA
XM_011545764.1:c.203-4503_203-4502delinsGA XP_011544066.1:n.203-4503_203-4502delinsGA
XM_011545765.1:c.203-4503_203-4502delinsGA XP_011544067.1:n.203-4503_203-4502delinsGA
XR_950754.1:n.457-4503_457-4502delinsGA
NM_174924.2:c.203-4503_203-4502delinsGA MANE Select NP_777584.1:n.203-4503_203-4502delinsGA