Canonical Allele Identifier: CA348591019

Gene: LCT

Linked Data

• MyVariant Identifiers: chr2:g.136555691A>C (hg19) ; chr2:g.135798121A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798121A>C , CM000664.2:g.135798121A>C	GRCh38
NC_000002.11:g.136555691A>C , CM000664.1:g.136555691A>C	GRCh37
NC_000002.10:g.136272161A>C	NCBI36
NG_008104.2:g.62049T>G , LRG_338:g.62049T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4884T>G MANE Select	ENSP00000264162.2:p.Phe1628Leu
ENST00000264162.6:c.4884T>G	ENSP00000264162.2:p.Phe1628Leu
ENST00000452974.1:c.2977T>G	ENSP00000391231.1:p.Cys993Gly
NM_002299.2:c.4884T>G , LRG_338t1:c.4884T>G	NP_002290.2:p.Phe1628Leu
NM_002299.3:c.4884T>G	NP_002290.2:p.Phe1628Leu
XM_017004088.2:c.4884T>G	XP_016859577.1:p.Phe1628Leu
NM_002299.4:c.4884T>G MANE Select	NP_002290.2:p.Phe1628Leu