Canonical Allele Identifier: CA1290822839

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135790046_135790047delinsGA , CM000664.2:g.135790046_135790047delinsGA	GRCh38
NC_000002.11:g.136547616_136547617delinsGA , CM000664.1:g.136547616_136547617delinsGA	GRCh37
NC_000002.10:g.136264086_136264087delinsGA	NCBI36
NG_008104.2:g.70123_70124delinsTC , LRG_338:g.70123_70124delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5336-249_5336-248delinsTC MANE Select	ENSP00000264162.2:n.5336-249_5336-248delinsTC
ENST00000264162.6:c.5336-249_5336-248delinsTC	ENSP00000264162.2:n.5336-249_5336-248delinsTC
NM_002299.2:c.5336-249_5336-248delinsTC , LRG_338t1:c.5336-249_5336-248delinsTC	NP_002290.2:n.5336-249_5336-248delinsTC
NM_002299.3:c.5336-249_5336-248delinsTC	NP_002290.2:n.5336-249_5336-248delinsTC
NM_002299.4:c.5336-249_5336-248delinsTC MANE Select	NP_002290.2:n.5336-249_5336-248delinsTC