Canonical Allele Identifier: CA348590830
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135798035T>G , CM000664.2:g.135798035T>G GRCh38
NC_000002.11:g.136555605T>G , CM000664.1:g.136555605T>G GRCh37
NC_000002.10:g.136272075T>G NCBI36
NG_008104.2:g.62135A>C , LRG_338:g.62135A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4970A>C MANE Select ENSP00000264162.2:p.Lys1657Thr
ENST00000264162.6:c.4970A>C ENSP00000264162.2:p.Lys1657Thr
ENST00000452974.1:c.3063A>C ENSP00000391231.1:n.3063A>C
NM_002299.2:c.4970A>C , LRG_338t1:c.4970A>C NP_002290.2:p.Lys1657Thr
NM_002299.3:c.4970A>C NP_002290.2:p.Lys1657Thr
XM_017004088.2:c.4970A>C XP_016859577.1:p.Lys1657Thr
NM_002299.4:c.4970A>C MANE Select NP_002290.2:p.Lys1657Thr