Canonical Allele Identifier: CA15882669
Gene: PDILT HGNC NCBI

Linked Data

dbSNP Id: rs11864909

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.20389517C>T , CM000678.2:g.20389517C>T GRCh38
NC_000016.9:g.20400839C>T , CM000678.1:g.20400839C>T GRCh37
NC_000016.8:g.20308340C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302451.9:c.203-4666G>A MANE Select ENSP00000305465.4:n.203-4666G>A
ENST00000302451.8:c.203-4666G>A ENSP00000305465.4:n.203-4666G>A
ENST00000575561.1:c.203-608G>A ENSP00000459161.1:n.203-608G>A
NM_174924.1:c.203-4666G>A NP_777584.1:n.203-4666G>A
XM_006721024.1:c.203-4666G>A XP_006721087.1:n.203-4666G>A
XM_011545764.1:c.203-4666G>A XP_011544066.1:n.203-4666G>A
XM_011545765.1:c.203-4666G>A XP_011544067.1:n.203-4666G>A
XR_950754.1:n.457-4666G>A
NM_174924.2:c.203-4666G>A MANE Select NP_777584.1:n.203-4666G>A