Canonical Allele Identifier: CA1290834597
Gene: LCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135816964G= , CM000664.2:g.135816964G= GRCh38
NC_000002.11:g.136574534G= , CM000664.1:g.136574534G= GRCh37
NC_000002.10:g.136291004G= NCBI36
NG_008104.2:g.43206C= , LRG_338:g.43206C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.1707+377C= MANE Select ENSP00000264162.2:n.1707+377C=
ENST00000264162.6:c.1707+377C= ENSP00000264162.2:n.1707+377C=
NM_002299.2:c.1707+377C= , LRG_338t1:c.1707+377C= NP_002290.2:n.1707+377C=
NM_002299.3:c.1707+377C= NP_002290.2:n.1707+377C=
XM_017004088.2:c.1707+377C= XP_016859577.1:n.1707+377C=
NM_002299.4:c.1707+377C= MANE Select NP_002290.2:n.1707+377C=
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