Canonical Allele Identifier: CA2480159084
Gene: LCE1C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152805856A= , CM000663.2:g.152805856A= GRCh38
NC_000001.10:g.152778332A= , CM000663.1:g.152778332A= GRCh37
NC_000001.9:g.151044956A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607093.2:c.-20-358T= MANE Select ENSP00000475270.1:n.-20-358T=
ENST00000606576.1:c.-20-358T= ENSP00000476034.1:n.-20-358T=
NM_001276331.1:c.-20-358T= NP_001263260.1:n.-20-358T=
NM_178351.3:c.-20-358T= NP_848128.1:n.-20-358T=
NM_001276331.2:c.-20-358T= NP_001263260.1:n.-20-358T=
NM_178351.4:c.-20-358T= MANE Select NP_848128.1:n.-20-358T=
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