Canonical Allele Identifier: CA2661274555

Gene: LCT

Linked Data

• gnomAD v4: 2-135798166-A-ACCTGTAACGCCTGGGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798166_135798167insCCTGTAACGCCTGGGCT , CM000664.2:g.135798166_135798167insCCTGTAACGCCTGGGCT	GRCh38
NC_000002.11:g.136555736_136555737insCCTGTAACGCCTGGGCT , CM000664.1:g.136555736_136555737insCCTGTAACGCCTGGGCT	GRCh37
NC_000002.10:g.136272206_136272207insCCTGTAACGCCTGGGCT	NCBI36
NG_008104.2:g.62003_62004insAGCCCAGGCGTTACAGG , LRG_338:g.62003_62004insAGCCCAGGCGTTACAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4867-29_4867-28insAGCCCAGGCGTTACAGG MANE Select	ENSP00000264162.2:n.4867-29_4867-28insAGCCCAGGCGTTACAGG
ENST00000264162.6:c.4867-29_4867-28insAGCCCAGGCGTTACAGG	ENSP00000264162.2:n.4867-29_4867-28insAGCCCAGGCGTTACAGG
ENST00000452974.1:c.2960-29_2960-28insAGCCCAGGCGTTACAGG	ENSP00000391231.1:n.2960-29_2960-28insAGCCCAGGCGTTACAGG
NM_002299.2:c.4867-29_4867-28insAGCCCAGGCGTTACAGG , LRG_338t1:c.4867-29_4867-28insAGCCCAGGCGTTACAGG	NP_002290.2:n.4867-29_4867-28insAGCCCAGGCGTTACAGG
NM_002299.3:c.4867-29_4867-28insAGCCCAGGCGTTACAGG	NP_002290.2:n.4867-29_4867-28insAGCCCAGGCGTTACAGG
XM_017004088.2:c.4867-29_4867-28insAGCCCAGGCGTTACAGG	XP_016859577.1:n.4867-29_4867-28insAGCCCAGGCGTTACAGG
NM_002299.4:c.4867-29_4867-28insAGCCCAGGCGTTACAGG MANE Select	NP_002290.2:n.4867-29_4867-28insAGCCCAGGCGTTACAGG