Canonical Allele Identifier: CA2661276787

Gene: LCT

Linked Data

• gnomAD v4: 2-135833339-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833340_135833341insCT , CM000664.2:g.135833340_135833341insCT	GRCh38
NC_000002.11:g.136590910_136590911insCT , CM000664.1:g.136590910_136590911insCT	GRCh37
NC_000002.10:g.136307380_136307381insCT	NCBI36
NG_008104.2:g.26830_26831insGA , LRG_338:g.26830_26831insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.641-150_641-149insGA MANE Select	ENSP00000264162.2:n.641-150_641-149insGA
ENST00000264162.6:c.641-150_641-149insGA	ENSP00000264162.2:n.641-150_641-149insGA
NM_002299.2:c.641-150_641-149insGA , LRG_338t1:c.641-150_641-149insGA	NP_002290.2:n.641-150_641-149insGA
NM_002299.3:c.641-150_641-149insGA	NP_002290.2:n.641-150_641-149insGA
XM_017004088.2:c.641-150_641-149insGA	XP_016859577.1:n.641-150_641-149insGA
NM_002299.4:c.641-150_641-149insGA MANE Select	NP_002290.2:n.641-150_641-149insGA