Canonical Allele Identifier: CA2577108121

Gene: LCT

Linked Data

• gnomAD v4: 2-135833257-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833262del , CM000664.2:g.135833262del	GRCh38
NC_000002.11:g.136590832del , CM000664.1:g.136590832del	GRCh37
NC_000002.10:g.136307302del	NCBI36
NG_008104.2:g.26912del , LRG_338:g.26912del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.641-68del MANE Select	ENSP00000264162.2:n.641-68del
ENST00000264162.6:c.641-68del	ENSP00000264162.2:n.641-68del
NM_002299.2:c.641-68del , LRG_338t1:c.641-68del	NP_002290.2:n.641-68del
NM_002299.3:c.641-68del	NP_002290.2:n.641-68del
XM_017004088.2:c.641-68del	XP_016859577.1:n.641-68del
NM_002299.4:c.641-68del MANE Select	NP_002290.2:n.641-68del