Canonical Allele Identifier: CA2661275728

Gene: LCT

Linked Data

• gnomAD v4: 2-135817284-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135817286del , CM000664.2:g.135817286del	GRCh38
NC_000002.11:g.136574856del , CM000664.1:g.136574856del	GRCh37
NC_000002.10:g.136291326del	NCBI36
NG_008104.2:g.42885del , LRG_338:g.42885del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.1707+56del MANE Select	ENSP00000264162.2:n.1707+56del
ENST00000264162.6:c.1707+56del	ENSP00000264162.2:n.1707+56del
NM_002299.2:c.1707+56del , LRG_338t1:c.1707+56del	NP_002290.2:n.1707+56del
NM_002299.3:c.1707+56del	NP_002290.2:n.1707+56del
XM_017004088.2:c.1707+56del	XP_016859577.1:n.1707+56del
NM_002299.4:c.1707+56del MANE Select	NP_002290.2:n.1707+56del