Canonical Allele Identifier: CA1290841259
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135833089T= , CM000664.2:g.135833089T= GRCh38
NC_000002.11:g.136590659T= , CM000664.1:g.136590659T= GRCh37
NC_000002.10:g.136307129T= NCBI36
NG_008104.2:g.27081A= , LRG_338:g.27081A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.720+22A= MANE Select ENSP00000264162.2:n.720+22A=
ENST00000264162.6:c.720+22A= ENSP00000264162.2:n.720+22A=
NM_002299.2:c.720+22A= , LRG_338t1:c.720+22A= NP_002290.2:n.720+22A=
NM_002299.3:c.720+22A= NP_002290.2:n.720+22A=
XM_017004088.2:c.720+22A= XP_016859577.1:n.720+22A=
NM_002299.4:c.720+22A= MANE Select NP_002290.2:n.720+22A=