Canonical Allele Identifier: CA1290841315

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833226_135833227delinsGA , CM000664.2:g.135833226_135833227delinsGA	GRCh38
NC_000002.11:g.136590796_136590797delinsGA , CM000664.1:g.136590796_136590797delinsGA	GRCh37
NC_000002.10:g.136307266_136307267delinsGA	NCBI36
NG_008104.2:g.26943_26944delinsTC , LRG_338:g.26943_26944delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.641-37_641-36delinsTC MANE Select	ENSP00000264162.2:n.641-37_641-36delinsTC
ENST00000264162.6:c.641-37_641-36delinsTC	ENSP00000264162.2:n.641-37_641-36delinsTC
NM_002299.2:c.641-37_641-36delinsTC , LRG_338t1:c.641-37_641-36delinsTC	NP_002290.2:n.641-37_641-36delinsTC
NM_002299.3:c.641-37_641-36delinsTC	NP_002290.2:n.641-37_641-36delinsTC
XM_017004088.2:c.641-37_641-36delinsTC	XP_016859577.1:n.641-37_641-36delinsTC
NM_002299.4:c.641-37_641-36delinsTC MANE Select	NP_002290.2:n.641-37_641-36delinsTC