Canonical Allele Identifier: CA1290841169

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135832815T= , CM000664.2:g.135832815T=	GRCh38
NC_000002.11:g.136590385T= , CM000664.1:g.136590385T=	GRCh37
NC_000002.10:g.136306855T=	NCBI36
NG_008104.2:g.27355A= , LRG_338:g.27355A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.720+296A= MANE Select	ENSP00000264162.2:n.720+296A=
ENST00000264162.6:c.720+296A=	ENSP00000264162.2:n.720+296A=
NM_002299.2:c.720+296A= , LRG_338t1:c.720+296A=	NP_002290.2:n.720+296A=
NM_002299.3:c.720+296A=	NP_002290.2:n.720+296A=
XM_017004088.2:c.720+296A=	XP_016859577.1:n.720+296A=
NM_002299.4:c.720+296A= MANE Select	NP_002290.2:n.720+296A=