Canonical Allele Identifier: CA402422138

Gene: LIPG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49582484T>C , CM000680.2:g.49582484T>C	GRCh38
NC_000018.9:g.47108854T>C , CM000680.1:g.47108854T>C	GRCh37
NC_000018.8:g.45362852T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261292.9:c.1157+2T>C MANE Select	ENSP00000261292.4:n.1157+2T>C
ENST00000261292.8:c.1157+2T>C	ENSP00000261292.4:n.1157+2T>C
ENST00000427224.6:c.935+2T>C	ENSP00000387978.2:n.935+2T>C
NM_001308006.1:c.935+2T>C	NP_001294935.1:n.935+2T>C
NM_006033.2:c.1157+2T>C	NP_006024.1:n.1157+2T>C
NM_006033.3:c.1157+2T>C	NP_006024.1:n.1157+2T>C
XM_005258390.1:c.1265+2T>C	XP_005258447.1:n.1265+2T>C
XM_011526265.1:c.1043+2T>C	XP_011524567.1:n.1043+2T>C
XM_011526267.1:c.917+2T>C	XP_011524569.1:n.917+2T>C
XM_011526265.3:c.1043+2T>C	XP_011524567.1:n.1043+2T>C
XM_017026095.1:c.566+2T>C	XP_016881584.1:n.566+2T>C
NM_006033.4:c.1157+2T>C MANE Select	NP_006024.1:n.1157+2T>C
NM_001308006.2:c.935+2T>C	NP_001294935.1:n.935+2T>C