Canonical Allele Identifier: CA1290834607

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135816992C= , CM000664.2:g.135816992C=	GRCh38
NC_000002.11:g.136574562C= , CM000664.1:g.136574562C=	GRCh37
NC_000002.10:g.136291032C=	NCBI36
NG_008104.2:g.43178G= , LRG_338:g.43178G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.1707+349G= MANE Select	ENSP00000264162.2:n.1707+349G=
ENST00000264162.6:c.1707+349G=	ENSP00000264162.2:n.1707+349G=
NM_002299.2:c.1707+349G= , LRG_338t1:c.1707+349G=	NP_002290.2:n.1707+349G=
NM_002299.3:c.1707+349G=	NP_002290.2:n.1707+349G=
XM_017004088.2:c.1707+349G=	XP_016859577.1:n.1707+349G=
NM_002299.4:c.1707+349G= MANE Select	NP_002290.2:n.1707+349G=