Canonical Allele Identifier: CA1290841275

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833142A= , CM000664.2:g.135833142A=	GRCh38
NC_000002.11:g.136590712A= , CM000664.1:g.136590712A=	GRCh37
NC_000002.10:g.136307182A=	NCBI36
NG_008104.2:g.27028T= , LRG_338:g.27028T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.689T= MANE Select	ENSP00000264162.2:p.Leu230=
ENST00000264162.6:c.689T=	ENSP00000264162.2:p.Leu230=
NM_002299.2:c.689T= , LRG_338t1:c.689T=	NP_002290.2:p.Leu230=
NM_002299.3:c.689T=	NP_002290.2:p.Leu230=
XM_017004088.2:c.689T=	XP_016859577.1:p.Leu230=
NM_002299.4:c.689T= MANE Select	NP_002290.2:p.Leu230=