Canonical Allele Identifier: CA1290822022
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788143G= , CM000664.2:g.135788143G= GRCh38
NC_000002.11:g.136545713G= , CM000664.1:g.136545713G= GRCh37
NC_000002.10:g.136262183G= NCBI36
NG_008104.2:g.72027C= , LRG_338:g.72027C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*181C= MANE Select ENSP00000264162.2:n.*181C=
ENST00000264162.6:c.*181C= ENSP00000264162.2:n.*181C=
NM_002299.2:c.*181C= , LRG_338t1:c.*181C= NP_002290.2:n.*181C=
NM_002299.3:c.*181C= NP_002290.2:n.*181C=
NM_002299.4:c.*181C= MANE Select NP_002290.2:n.*181C=