Canonical Allele Identifier: CA1290829338

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135804824G= , CM000664.2:g.135804824G=	GRCh38
NC_000002.11:g.136562394G= , CM000664.1:g.136562394G=	GRCh37
NC_000002.10:g.136278864G=	NCBI36
NG_008104.2:g.55346C= , LRG_338:g.55346C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264162.7:c.4407C= MANE Select	ENSP00000264162.2:p.Gly1469=
ENST00000264162.6:c.4407C=	ENSP00000264162.2:p.Gly1469=
ENST00000452974.1:c.2703C=	ENSP00000391231.1:p.Gly901=
NM_002299.2:c.4407C= , LRG_338t1:c.4407C=	NP_002290.2:p.Gly1469=
NM_002299.3:c.4407C=	NP_002290.2:p.Gly1469=
XM_017004088.2:c.4407C=	XP_016859577.1:p.Gly1469=
NM_002299.4:c.4407C= MANE Select	NP_002290.2:p.Gly1469=