Canonical Allele Identifier: CA1290827719

Gene: LCT

Linked Data

• dbSNP Id: rs2077621858

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800977_135800983dup , CM000664.2:g.135800977_135800983dup	GRCh38
NC_000002.11:g.136558547_136558553dup , CM000664.1:g.136558547_136558553dup	GRCh37
NC_000002.10:g.136275017_136275023dup	NCBI36
NG_008104.2:g.59187_59193dup , LRG_338:g.59187_59193dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4664-174_4664-168dup MANE Select	ENSP00000264162.2:n.4664-174_4664-168dup
ENST00000264162.6:c.4664-174_4664-168dup	ENSP00000264162.2:n.4664-174_4664-168dup
ENST00000452974.1:c.2960-2845_2960-2839dup	ENSP00000391231.1:n.2960-2845_2960-2839dup
NM_002299.2:c.4664-174_4664-168dup , LRG_338t1:c.4664-174_4664-168dup	NP_002290.2:n.4664-174_4664-168dup
NM_002299.3:c.4664-174_4664-168dup	NP_002290.2:n.4664-174_4664-168dup
XM_017004088.2:c.4664-174_4664-168dup	XP_016859577.1:n.4664-174_4664-168dup
NM_002299.4:c.4664-174_4664-168dup MANE Select	NP_002290.2:n.4664-174_4664-168dup