Canonical Allele Identifier: CA1290834798

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135817477G= , CM000664.2:g.135817477G=	GRCh38
NC_000002.11:g.136575047G= , CM000664.1:g.136575047G=	GRCh37
NC_000002.10:g.136291517G=	NCBI36
NG_008104.2:g.42693C= , LRG_338:g.42693C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264162.7:c.1571C= MANE Select	ENSP00000264162.2:p.Ala524=
ENST00000264162.6:c.1571C=	ENSP00000264162.2:p.Ala524=
NM_002299.2:c.1571C= , LRG_338t1:c.1571C=	NP_002290.2:p.Ala524=
NM_002299.3:c.1571C=	NP_002290.2:p.Ala524=
XM_017004088.2:c.1571C=	XP_016859577.1:p.Ala524=
NM_002299.4:c.1571C= MANE Select	NP_002290.2:p.Ala524=