Canonical Allele Identifier: CA1290841175

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135832825_135832830delinsTTTGCC , CM000664.2:g.135832825_135832830delinsTTTGCC	GRCh38
NC_000002.11:g.136590395_136590400delinsTTTGCC , CM000664.1:g.136590395_136590400delinsTTTGCC	GRCh37
NC_000002.10:g.136306865_136306870delinsTTTGCC	NCBI36
NG_008104.2:g.27340_27345delinsGGCAAA , LRG_338:g.27340_27345delinsGGCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.720+281_720+286delinsGGCAAA MANE Select	ENSP00000264162.2:n.720+281_720+286delinsGGCAAA
ENST00000264162.6:c.720+281_720+286delinsGGCAAA	ENSP00000264162.2:n.720+281_720+286delinsGGCAAA
NM_002299.2:c.720+281_720+286delinsGGCAAA , LRG_338t1:c.720+281_720+286delinsGGCAAA	NP_002290.2:n.720+281_720+286delinsGGCAAA
NM_002299.3:c.720+281_720+286delinsGGCAAA	NP_002290.2:n.720+281_720+286delinsGGCAAA
XM_017004088.2:c.720+281_720+286delinsGGCAAA	XP_016859577.1:n.720+281_720+286delinsGGCAAA
NM_002299.4:c.720+281_720+286delinsGGCAAA MANE Select	NP_002290.2:n.720+281_720+286delinsGGCAAA