Canonical Allele Identifier: CA1290821934

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135787954T= , CM000664.2:g.135787954T=	GRCh38
NC_000002.11:g.136545524T= , CM000664.1:g.136545524T=	GRCh37
NC_000002.10:g.136261994T=	NCBI36
NG_008104.2:g.72216A= , LRG_338:g.72216A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.*370A= MANE Select	ENSP00000264162.2:n.*370A=
ENST00000264162.6:c.*370A=	ENSP00000264162.2:n.*370A=
NM_002299.2:c.*370A= , LRG_338t1:c.*370A=	NP_002290.2:n.*370A=
NM_002299.3:c.*370A=	NP_002290.2:n.*370A=
NM_002299.4:c.*370A= MANE Select	NP_002290.2:n.*370A=