Canonical Allele Identifier: CA1290822685

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135789668C= , CM000664.2:g.135789668C=	GRCh38
NC_000002.11:g.136547238C= , CM000664.1:g.136547238C=	GRCh37
NC_000002.10:g.136263708C=	NCBI36
NG_008104.2:g.70502G= , LRG_338:g.70502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5466G= MANE Select	ENSP00000264162.2:p.Arg1822=
ENST00000264162.6:c.5466G=	ENSP00000264162.2:p.Arg1822=
NM_002299.2:c.5466G= , LRG_338t1:c.5466G=	NP_002290.2:p.Arg1822=
NM_002299.3:c.5466G=	NP_002290.2:p.Arg1822=
NM_002299.4:c.5466G= MANE Select	NP_002290.2:p.Arg1822=