Canonical Allele Identifier: CA1290826532
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135798100A= , CM000664.2:g.135798100A= GRCh38
NC_000002.11:g.136555670A= , CM000664.1:g.136555670A= GRCh37
NC_000002.10:g.136272140A= NCBI36
NG_008104.2:g.62070T= , LRG_338:g.62070T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4905T= MANE Select ENSP00000264162.2:p.Asn1635=
ENST00000264162.6:c.4905T= ENSP00000264162.2:p.Asn1635=
ENST00000452974.1:c.2998T= ENSP00000391231.1:p.Trp1000=
NM_002299.2:c.4905T= , LRG_338t1:c.4905T= NP_002290.2:p.Asn1635=
NM_002299.3:c.4905T= NP_002290.2:p.Asn1635=
XM_017004088.2:c.4905T= XP_016859577.1:p.Asn1635=
NM_002299.4:c.4905T= MANE Select NP_002290.2:p.Asn1635=