Canonical Allele Identifier: CA2661274927

Gene: LCT

Linked Data

• gnomAD v4: 2-135800874-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800874_135800875insA , CM000664.2:g.135800874_135800875insA	GRCh38
NC_000002.11:g.136558444_136558445insA , CM000664.1:g.136558444_136558445insA	GRCh37
NC_000002.10:g.136274914_136274915insA	NCBI36
NG_008104.2:g.59295_59296insT , LRG_338:g.59295_59296insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4664-66_4664-65insT MANE Select	ENSP00000264162.2:n.4664-66_4664-65insT
ENST00000264162.6:c.4664-66_4664-65insT	ENSP00000264162.2:n.4664-66_4664-65insT
ENST00000452974.1:c.2960-2737_2960-2736insT	ENSP00000391231.1:n.2960-2737_2960-2736insT
NM_002299.2:c.4664-66_4664-65insT , LRG_338t1:c.4664-66_4664-65insT	NP_002290.2:n.4664-66_4664-65insT
NM_002299.3:c.4664-66_4664-65insT	NP_002290.2:n.4664-66_4664-65insT
XM_017004088.2:c.4664-66_4664-65insT	XP_016859577.1:n.4664-66_4664-65insT
NM_002299.4:c.4664-66_4664-65insT MANE Select	NP_002290.2:n.4664-66_4664-65insT