Canonical Allele Identifier: CA383946439

Gene: LRP6 BCL2L14

Linked Data

• MyVariant Identifiers: chr12:g.12317284T>C (hg19) ; chr12:g.12164350T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12164350T>C , CM000674.2:g.12164350T>C	GRCh38
NC_000012.11:g.12317284T>C , CM000674.1:g.12317284T>C	GRCh37
NC_000012.10:g.12208551T>C	NCBI36
NG_016168.1:g.107528A>G
NG_016168.2:g.107528A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261349.9:c.1975A>G (LRP6) MANE Select	ENSP00000261349.4:p.Thr659Ala
ENST00000261349.8:c.1975A>G (LRP6)	ENSP00000261349.4:p.Thr659Ala
ENST00000298566.2:c.*25-22955T>C (BCL2L14)	ENSP00000298566.1:n.*25-22955T>C
ENST00000538239.5:c.1569A>G (LRP6)
ENST00000543091.1:c.1975A>G (LRP6)	ENSP00000442472.1:p.Thr659Ala
NM_002336.2:c.1975A>G (LRP6)	NP_002327.2:p.Thr659Ala
XM_006719078.2:c.1975A>G (LRP6)	XP_006719141.1:p.Thr659Ala
XM_011520671.1:c.1522A>G (LRP6)	XP_011518973.1:p.Thr508Ala
XR_429034.1:n.2108A>G (LRP6)
XR_429035.1:n.2108A>G (LRP6)
XM_006719078.4:c.1975A>G (LRP6)	XP_006719141.1:p.Thr659Ala
XM_011520671.3:c.1522A>G (LRP6)	XP_011518973.1:p.Thr508Ala
XR_002957325.1:n.2108A>G (LRP6)
XR_429035.3:n.2108A>G (LRP6)
NM_002336.3:c.1975A>G (LRP6) MANE Select	NP_002327.2:p.Thr659Ala