Canonical Allele Identifier: CA1290826465
Gene: LCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135797923G= , CM000664.2:g.135797923G= GRCh38
NC_000002.11:g.136555493G= , CM000664.1:g.136555493G= GRCh37
NC_000002.10:g.136271963G= NCBI36
NG_008104.2:g.62247C= , LRG_338:g.62247C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4976+106C= MANE Select ENSP00000264162.2:n.4976+106C=
ENST00000264162.6:c.4976+106C= ENSP00000264162.2:n.4976+106C=
ENST00000452974.1:c.3069+106C= ENSP00000391231.1:n.3069+106C=
NM_002299.2:c.4976+106C= , LRG_338t1:c.4976+106C= NP_002290.2:n.4976+106C=
NM_002299.3:c.4976+106C= NP_002290.2:n.4976+106C=
XM_017004088.2:c.4976+106C= XP_016859577.1:n.4976+106C=
NM_002299.4:c.4976+106C= MANE Select NP_002290.2:n.4976+106C=
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