Canonical Allele Identifier: CA1290826544

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798144G= , CM000664.2:g.135798144G=	GRCh38
NC_000002.11:g.136555714G= , CM000664.1:g.136555714G=	GRCh37
NC_000002.10:g.136272184G=	NCBI36
NG_008104.2:g.62026C= , LRG_338:g.62026C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4867-6C= MANE Select	ENSP00000264162.2:n.4867-6C=
ENST00000264162.6:c.4867-6C=	ENSP00000264162.2:n.4867-6C=
ENST00000452974.1:c.2960-6C=	ENSP00000391231.1:n.2960-6C=
NM_002299.2:c.4867-6C= , LRG_338t1:c.4867-6C=	NP_002290.2:n.4867-6C=
NM_002299.3:c.4867-6C=	NP_002290.2:n.4867-6C=
XM_017004088.2:c.4867-6C=	XP_016859577.1:n.4867-6C=
NM_002299.4:c.4867-6C= MANE Select	NP_002290.2:n.4867-6C=