Canonical Allele Identifier: CA2231493877
Community Standard Title: NM_181536.2(PKD1L3):c.4927-1110G=
Gene: PKD1L3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.71931293C= , CM000678.2:g.71931293C= GRCh38
NC_000016.9:g.71965196C= , CM000678.1:g.71965196C= GRCh37
NC_000016.8:g.70522697C= NCBI36
NG_032958.1:g.73686G=

Transcript Alleles

HGVS Amino-acid Change
NM_181536.2:c.4927-1110G= MANE Select NP_853514.1:n.4927-1110G=
ENST00000620267.2:c.4927-1110G= MANE Select ENSP00000480090.1:n.4927-1110G=
NM_181536.1:c.4927-1110G= NP_853514.1:n.4927-1110G=
ENST00000620267.1:c.4927-1110G= ENSP00000480090.1:n.4927-1110G=
XM_024450254.1:c.4924-1110G= XP_024306022.1:n.4924-1110G=
XM_024450255.1:c.4909-1110G= XP_024306023.1:n.4909-1110G=
XM_024450256.1:c.4750-1110G= XP_024306024.1:n.4750-1110G=
XM_024450257.1:c.4741-1110G= XP_024306025.1:n.4741-1110G=
XM_024450258.1:c.4375-1110G= XP_024306026.1:n.4375-1110G=
XM_024450259.1:c.4375-1110G= XP_024306027.1:n.4375-1110G=
XM_024450260.1:c.4219-1110G= XP_024306028.1:n.4219-1110G=