Canonical Allele Identifier: CA1290827629

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800720C= , CM000664.2:g.135800720C=	GRCh38
NC_000002.11:g.136558290C= , CM000664.1:g.136558290C=	GRCh37
NC_000002.10:g.136274760C=	NCBI36
NG_008104.2:g.59450G= , LRG_338:g.59450G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4753G= MANE Select	ENSP00000264162.2:p.Val1585=
ENST00000264162.6:c.4753G=	ENSP00000264162.2:p.Val1585=
ENST00000452974.1:c.2960-2582G=	ENSP00000391231.1:n.2960-2582G=
NM_002299.2:c.4753G= , LRG_338t1:c.4753G=	NP_002290.2:p.Val1585=
NM_002299.3:c.4753G=	NP_002290.2:p.Val1585=
XM_017004088.2:c.4753G=	XP_016859577.1:p.Val1585=
NM_002299.4:c.4753G= MANE Select	NP_002290.2:p.Val1585=