Canonical Allele Identifier: CA1413585361

Gene: LEKR1

Linked Data

• dbSNP Id: rs12638253

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.156908302C>G , CM000665.2:g.156908302C>G	GRCh38
NC_000003.11:g.156626091C>G , CM000665.1:g.156626091C>G	GRCh37
NC_000003.10:g.158108785C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356539.9:c.264-12273C>G MANE Select	ENSP00000348936.4:n.264-12273C>G
ENST00000470811.6:c.264-12273C>G	ENSP00000418214.2:n.264-12273C>G
ENST00000356539.8:c.264-12273C>G	ENSP00000348936.4:n.264-12273C>G
ENST00000467376.5:n.136-12273C>G
ENST00000470811.5:c.-958-12273C>G	ENSP00000418214.1:n.-958-12273C>G
ENST00000477399.5:c.264-12273C>G	ENSP00000425282.1:n.264-12273C>G
ENST00000489350.5:n.141-12273C>G
ENST00000491763.1:c.264-12273C>G	ENSP00000474182.1:n.264-12273C>G
NM_001004316.2:c.264-12273C>G	NP_001004316.2:n.264-12273C>G
NM_001193283.1:c.264-12273C>G	NP_001180212.1:n.264-12273C>G
XM_005247441.2:c.264-12273C>G	XP_005247498.1:n.264-12273C>G
XM_005247442.2:c.264-12273C>G	XP_005247499.1:n.264-12273C>G
XM_006713631.2:c.765-12273C>G	XP_006713694.1:n.765-12273C>G
XM_006713632.2:c.765-12273C>G	XP_006713695.1:n.765-12273C>G
XM_011512803.1:c.765-12273C>G	XP_011511105.1:n.765-12273C>G
XM_011512804.1:c.264-12273C>G	XP_011511106.1:n.264-12273C>G
XM_011512805.1:c.-16-12273C>G	XP_011511107.1:n.-16-12273C>G
XM_011512806.1:c.765-12273C>G	XP_011511108.1:n.765-12273C>G
XM_011512807.1:c.765-12273C>G	XP_011511109.1:n.765-12273C>G
XM_011512808.1:c.765-12273C>G	XP_011511110.1:n.765-12273C>G
XM_011512810.1:c.-65-34227C>G	XP_011511112.1:n.-65-34227C>G
XM_011512811.1:c.765-12273C>G	XP_011511113.1:n.765-12273C>G
XM_011512812.1:c.765-12273C>G	XP_011511114.1:n.765-12273C>G
XM_011512814.1:c.-56-70892C>G	XP_011511116.1:n.-56-70892C>G
XM_011512815.1:c.765-12273C>G	XP_011511117.1:n.765-12273C>G
XM_011512816.1:c.765-12273C>G	XP_011511118.1:n.765-12273C>G
XR_924134.1:n.806-12273C>G
XR_924135.1:n.806-12273C>G
XM_005247441.4:c.264-12273C>G	XP_005247498.1:n.264-12273C>G
XM_005247442.4:c.264-12273C>G	XP_005247499.1:n.264-12273C>G
XM_006713631.3:c.765-12273C>G	XP_006713694.1:n.765-12273C>G
XM_011512803.2:c.765-12273C>G	XP_011511105.1:n.765-12273C>G
XM_011512804.3:c.264-12273C>G	XP_011511106.1:n.264-12273C>G
XM_011512806.2:c.765-12273C>G	XP_011511108.1:n.765-12273C>G
XM_011512807.2:c.765-12273C>G	XP_011511109.1:n.765-12273C>G
XM_011512808.2:c.765-12273C>G	XP_011511110.1:n.765-12273C>G
XM_011512811.2:c.765-12273C>G	XP_011511113.1:n.765-12273C>G
XM_011512814.2:c.-56-70892C>G	XP_011511116.1:n.-56-70892C>G
XM_011512815.2:c.765-12273C>G	XP_011511117.1:n.765-12273C>G
XM_011512816.2:c.765-12273C>G	XP_011511118.1:n.765-12273C>G
XM_017006375.1:c.-65-34227C>G	XP_016861864.1:n.-65-34227C>G
XR_924134.2:n.902-12273C>G
XR_924135.3:n.902-12273C>G
NM_001193283.2:c.264-12273C>G	NP_001180212.1:n.264-12273C>G
NM_001004316.3:c.264-12273C>G MANE Select	NP_001004316.2:n.264-12273C>G