Canonical Allele Identifier: CA1290827534

Gene: LCT

Linked Data

• dbSNP Id: rs2077616382
• gnomAD v4: 2-135800482-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800484del , CM000664.2:g.135800484del	GRCh38
NC_000002.11:g.136558054del , CM000664.1:g.136558054del	GRCh37
NC_000002.10:g.136274524del	NCBI36
NG_008104.2:g.59687del , LRG_338:g.59687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4866+124del MANE Select	ENSP00000264162.2:n.4866+124del
ENST00000264162.6:c.4866+124del	ENSP00000264162.2:n.4866+124del
ENST00000452974.1:c.2960-2345del	ENSP00000391231.1:n.2960-2345del
NM_002299.2:c.4866+124del , LRG_338t1:c.4866+124del	NP_002290.2:n.4866+124del
NM_002299.3:c.4866+124del	NP_002290.2:n.4866+124del
XM_017004088.2:c.4866+124del	XP_016859577.1:n.4866+124del
NM_002299.4:c.4866+124del MANE Select	NP_002290.2:n.4866+124del