Canonical Allele Identifier: CA1290834614

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135817000G= , CM000664.2:g.135817000G=	GRCh38
NC_000002.11:g.136574570G= , CM000664.1:g.136574570G=	GRCh37
NC_000002.10:g.136291040G=	NCBI36
NG_008104.2:g.43170C= , LRG_338:g.43170C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.1707+341C= MANE Select	ENSP00000264162.2:n.1707+341C=
ENST00000264162.6:c.1707+341C=	ENSP00000264162.2:n.1707+341C=
NM_002299.2:c.1707+341C= , LRG_338t1:c.1707+341C=	NP_002290.2:n.1707+341C=
NM_002299.3:c.1707+341C=	NP_002290.2:n.1707+341C=
XM_017004088.2:c.1707+341C=	XP_016859577.1:n.1707+341C=
NM_002299.4:c.1707+341C= MANE Select	NP_002290.2:n.1707+341C=