Canonical Allele Identifier: CA1290821954

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135787986C= , CM000664.2:g.135787986C=	GRCh38
NC_000002.11:g.136545556C= , CM000664.1:g.136545556C=	GRCh37
NC_000002.10:g.136262026C=	NCBI36
NG_008104.2:g.72184G= , LRG_338:g.72184G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.*338G= MANE Select	ENSP00000264162.2:n.*338G=
ENST00000264162.6:c.*338G=	ENSP00000264162.2:n.*338G=
NM_002299.2:c.*338G= , LRG_338t1:c.*338G=	NP_002290.2:n.*338G=
NM_002299.3:c.*338G=	NP_002290.2:n.*338G=
NM_002299.4:c.*338G= MANE Select	NP_002290.2:n.*338G=