Canonical Allele Identifier: CA2661271129

Gene: LCT

Linked Data

• gnomAD v4: 2-135787929-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135787929T>A , CM000664.2:g.135787929T>A	GRCh38
NC_000002.11:g.136545499T>A , CM000664.1:g.136545499T>A	GRCh37
NC_000002.10:g.136261969T>A	NCBI36
NG_008104.2:g.72241A>T , LRG_338:g.72241A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.*395A>T MANE Select	ENSP00000264162.2:n.*395A>T
ENST00000264162.6:c.*395A>T	ENSP00000264162.2:n.*395A>T
NM_002299.2:c.*395A>T , LRG_338t1:c.*395A>T	NP_002290.2:n.*395A>T
NM_002299.3:c.*395A>T	NP_002290.2:n.*395A>T
NM_002299.4:c.*395A>T MANE Select	NP_002290.2:n.*395A>T