Canonical Allele Identifier: CA1290826485
Gene: LCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135797984A= , CM000664.2:g.135797984A= GRCh38
NC_000002.11:g.136555554A= , CM000664.1:g.136555554A= GRCh37
NC_000002.10:g.136272024A= NCBI36
NG_008104.2:g.62186T= , LRG_338:g.62186T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4976+45T= MANE Select ENSP00000264162.2:n.4976+45T=
ENST00000264162.6:c.4976+45T= ENSP00000264162.2:n.4976+45T=
ENST00000452974.1:c.3069+45T= ENSP00000391231.1:n.3069+45T=
NM_002299.2:c.4976+45T= , LRG_338t1:c.4976+45T= NP_002290.2:n.4976+45T=
NM_002299.3:c.4976+45T= NP_002290.2:n.4976+45T=
XM_017004088.2:c.4976+45T= XP_016859577.1:n.4976+45T=
NM_002299.4:c.4976+45T= MANE Select NP_002290.2:n.4976+45T=
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