Canonical Allele Identifier: CA1290821924
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787924G= , CM000664.2:g.135787924G= GRCh38
NC_000002.11:g.136545494G= , CM000664.1:g.136545494G= GRCh37
NC_000002.10:g.136261964G= NCBI36
NG_008104.2:g.72246C= , LRG_338:g.72246C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.*400C= MANE Select ENSP00000264162.2:n.*400C=
ENST00000264162.6:c.*400C= ENSP00000264162.2:n.*400C=
NM_002299.2:c.*400C= , LRG_338t1:c.*400C= NP_002290.2:n.*400C=
NM_002299.3:c.*400C= NP_002290.2:n.*400C=
NM_002299.4:c.*400C= MANE Select NP_002290.2:n.*400C=