Canonical Allele Identifier: CA348590970
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135798101T>C , CM000664.2:g.135798101T>C GRCh38
NC_000002.11:g.136555671T>C , CM000664.1:g.136555671T>C GRCh37
NC_000002.10:g.136272141T>C NCBI36
NG_008104.2:g.62069A>G , LRG_338:g.62069A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4904A>G MANE Select ENSP00000264162.2:p.Asn1635Ser
ENST00000264162.6:c.4904A>G ENSP00000264162.2:p.Asn1635Ser
ENST00000452974.1:c.2997A>G ENSP00000391231.1:p.Glu999=
NM_002299.2:c.4904A>G , LRG_338t1:c.4904A>G NP_002290.2:p.Asn1635Ser
NM_002299.3:c.4904A>G NP_002290.2:p.Asn1635Ser
XM_017004088.2:c.4904A>G XP_016859577.1:p.Asn1635Ser
NM_002299.4:c.4904A>G MANE Select NP_002290.2:p.Asn1635Ser