Canonical Allele Identifier: CA507294110
Gene: LGI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.35617791G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35126887G>A , CM000681.2:g.35126887G>A GRCh38
NC_000019.9:g.35617791G>A , CM000681.1:g.35617791G>A GRCh37
NC_000019.8:g.40309631G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310123.8:c.759C>T MANE Select ENSP00000312273.3:p.Ser253=
ENST00000310123.7:c.759C>T ENSP00000312273.3:p.Ser253=
ENST00000392225.7:c.759C>T ENSP00000376059.3:p.Ser253=
ENST00000493050.5:n.818C>T
ENST00000587780.5:c.494C>T
ENST00000591840.5:n.420-2021C>T
ENST00000593248.5:n.890C>T
NM_139284.2:c.759C>T NP_644813.1:p.Ser253=
XM_011526594.1:c.759C>T XP_011524896.1:p.Ser253=
XM_011526595.1:c.243C>T XP_011524897.1:p.Ser81=
XM_011526595.2:c.243C>T XP_011524897.1:p.Ser81=
XM_017026428.1:c.243C>T XP_016881917.1:p.Ser81=
XM_017026429.1:c.243C>T XP_016881918.1:p.Ser81=
XM_017026430.2:c.243C>T XP_016881919.1:p.Ser81=
NM_139284.3:c.759C>T MANE Select NP_644813.1:p.Ser253=