Canonical Allele Identifier: CA2661274562

Gene: LCT

Linked Data

• gnomAD v4: 2-135798172-TACAGGTGGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798177_135798186del , CM000664.2:g.135798177_135798186del	GRCh38
NC_000002.11:g.136555747_136555756del , CM000664.1:g.136555747_136555756del	GRCh37
NC_000002.10:g.136272217_136272226del	NCBI36
NG_008104.2:g.61988_61997del , LRG_338:g.61988_61997del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4867-44_4867-35del MANE Select	ENSP00000264162.2:n.4867-44_4867-35del
ENST00000264162.6:c.4867-44_4867-35del	ENSP00000264162.2:n.4867-44_4867-35del
ENST00000452974.1:c.2960-44_2960-35del	ENSP00000391231.1:n.2960-44_2960-35del
NM_002299.2:c.4867-44_4867-35del , LRG_338t1:c.4867-44_4867-35del	NP_002290.2:n.4867-44_4867-35del
NM_002299.3:c.4867-44_4867-35del	NP_002290.2:n.4867-44_4867-35del
XM_017004088.2:c.4867-44_4867-35del	XP_016859577.1:n.4867-44_4867-35del
NM_002299.4:c.4867-44_4867-35del MANE Select	NP_002290.2:n.4867-44_4867-35del