Canonical Allele Identifier: CA2480159144
Gene: LCE1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152805983T= , CM000663.2:g.152805983T= GRCh38
NC_000001.10:g.152778459T= , CM000663.1:g.152778459T= GRCh37
NC_000001.9:g.151045083T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000607093.2:c.-20-485A= MANE Select ENSP00000475270.1:n.-20-485A=
ENST00000606576.1:c.-20-485A= ENSP00000476034.1:n.-20-485A=
NM_001276331.1:c.-20-485A= NP_001263260.1:n.-20-485A=
NM_178351.3:c.-20-485A= NP_848128.1:n.-20-485A=
NM_001276331.2:c.-20-485A= NP_001263260.1:n.-20-485A=
NM_178351.4:c.-20-485A= MANE Select NP_848128.1:n.-20-485A=