Canonical Allele Identifier: CA2577108113

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833231del , CM000664.2:g.135833231del	GRCh38
NC_000002.11:g.136590801del , CM000664.1:g.136590801del	GRCh37
NC_000002.10:g.136307271del	NCBI36
NG_008104.2:g.26939del , LRG_338:g.26939del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.641-41del MANE Select	ENSP00000264162.2:n.641-41del
ENST00000264162.6:c.641-41del	ENSP00000264162.2:n.641-41del
NM_002299.2:c.641-41del , LRG_338t1:c.641-41del	NP_002290.2:n.641-41del
NM_002299.3:c.641-41del	NP_002290.2:n.641-41del
XM_017004088.2:c.641-41del	XP_016859577.1:n.641-41del
NM_002299.4:c.641-41del MANE Select	NP_002290.2:n.641-41del