Canonical Allele Identifier: CA1616492500
Gene: GPLD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24491187C= , CM000668.2:g.24491187C= GRCh38
NC_000006.11:g.24491415C= , CM000668.1:g.24491415C= GRCh37
NC_000006.10:g.24599394C= NCBI36
NG_008161.1:g.1219C=
NG_029888.2:g.3436G=

Transcript Alleles

HGVS Amino-acid change
ENST00000474784.5:n.240-1690G=
ENST00000475417.1:n.234-1690G=
XM_011514509.1:c.45-1690G= XP_011512811.1:n.45-1690G=
XM_017010753.2:c.45-1690G= XP_016866242.1:n.45-1690G=
XR_002956277.1:n.267-1690G=