Canonical Allele Identifier: CA1290834794
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135817461T= , CM000664.2:g.135817461T= GRCh38
NC_000002.11:g.136575031T= , CM000664.1:g.136575031T= GRCh37
NC_000002.10:g.136291501T= NCBI36
NG_008104.2:g.42709A= , LRG_338:g.42709A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.1587A= MANE Select ENSP00000264162.2:p.Thr529=
ENST00000264162.6:c.1587A= ENSP00000264162.2:p.Thr529=
NM_002299.2:c.1587A= , LRG_338t1:c.1587A= NP_002290.2:p.Thr529=
NM_002299.3:c.1587A= NP_002290.2:p.Thr529=
XM_017004088.2:c.1587A= XP_016859577.1:p.Thr529=
NM_002299.4:c.1587A= MANE Select NP_002290.2:p.Thr529=