Canonical Allele Identifier: CA348590925

Gene: LCT

Linked Data

• MyVariant Identifiers: chr2:g.136555651T>G (hg19) ; chr2:g.135798081T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798081T>G , CM000664.2:g.135798081T>G	GRCh38
NC_000002.11:g.136555651T>G , CM000664.1:g.136555651T>G	GRCh37
NC_000002.10:g.136272121T>G	NCBI36
NG_008104.2:g.62089A>C , LRG_338:g.62089A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4924A>C MANE Select	ENSP00000264162.2:p.Met1642Leu
ENST00000264162.6:c.4924A>C	ENSP00000264162.2:p.Met1642Leu
ENST00000452974.1:c.3017A>C	ENSP00000391231.1:n.3017A>C
NM_002299.2:c.4924A>C , LRG_338t1:c.4924A>C	NP_002290.2:p.Met1642Leu
NM_002299.3:c.4924A>C	NP_002290.2:p.Met1642Leu
XM_017004088.2:c.4924A>C	XP_016859577.1:p.Met1642Leu
NM_002299.4:c.4924A>C MANE Select	NP_002290.2:p.Met1642Leu