Canonical Allele Identifier: CA2752322927

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833037del , CM000664.2:g.135833037del	GRCh38
NC_000002.11:g.136590607del , CM000664.1:g.136590607del	GRCh37
NC_000002.10:g.136307077del	NCBI36
NG_008104.2:g.27136del , LRG_338:g.27136del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.720+77del MANE Select	ENSP00000264162.2:n.720+77del
ENST00000264162.6:c.720+77del	ENSP00000264162.2:n.720+77del
NM_002299.2:c.720+77del , LRG_338t1:c.720+77del	NP_002290.2:n.720+77del
NM_002299.3:c.720+77del	NP_002290.2:n.720+77del
XM_017004088.2:c.720+77del	XP_016859577.1:n.720+77del
NM_002299.4:c.720+77del MANE Select	NP_002290.2:n.720+77del