Canonical Allele Identifier: CA1290826537

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798121A= , CM000664.2:g.135798121A=	GRCh38
NC_000002.11:g.136555691A= , CM000664.1:g.136555691A=	GRCh37
NC_000002.10:g.136272161A=	NCBI36
NG_008104.2:g.62049T= , LRG_338:g.62049T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264162.7:c.4884T= MANE Select	ENSP00000264162.2:p.Phe1628=
ENST00000264162.6:c.4884T=	ENSP00000264162.2:p.Phe1628=
ENST00000452974.1:c.2977T=	ENSP00000391231.1:p.Cys993=
NM_002299.2:c.4884T= , LRG_338t1:c.4884T=	NP_002290.2:p.Phe1628=
NM_002299.3:c.4884T=	NP_002290.2:p.Phe1628=
XM_017004088.2:c.4884T=	XP_016859577.1:p.Phe1628=
NM_002299.4:c.4884T= MANE Select	NP_002290.2:p.Phe1628=