Canonical Allele Identifier: CA1290834618

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135817019A= , CM000664.2:g.135817019A=	GRCh38
NC_000002.11:g.136574589A= , CM000664.1:g.136574589A=	GRCh37
NC_000002.10:g.136291059A=	NCBI36
NG_008104.2:g.43151T= , LRG_338:g.43151T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.1707+322T= MANE Select	ENSP00000264162.2:n.1707+322T=
ENST00000264162.6:c.1707+322T=	ENSP00000264162.2:n.1707+322T=
NM_002299.2:c.1707+322T= , LRG_338t1:c.1707+322T=	NP_002290.2:n.1707+322T=
NM_002299.3:c.1707+322T=	NP_002290.2:n.1707+322T=
XM_017004088.2:c.1707+322T=	XP_016859577.1:n.1707+322T=
NM_002299.4:c.1707+322T= MANE Select	NP_002290.2:n.1707+322T=