Canonical Allele Identifier: CA8959324

Gene: LIPG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49583552G>C , CM000680.2:g.49583552G>C	GRCh38
NC_000018.9:g.47109922G>C , CM000680.1:g.47109922G>C	GRCh37
NC_000018.8:g.45363920G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261292.9:c.1158-4G>C MANE Select	ENSP00000261292.4:n.1158-4G>C
ENST00000261292.8:c.1158-4G>C	ENSP00000261292.4:n.1158-4G>C
ENST00000427224.6:c.936-4G>C	ENSP00000387978.2:n.936-4G>C
NM_001308006.1:c.936-4G>C	NP_001294935.1:n.936-4G>C
NM_006033.2:c.1158-4G>C	NP_006024.1:n.1158-4G>C
NM_006033.3:c.1158-4G>C	NP_006024.1:n.1158-4G>C
XM_005258390.1:c.1266-4G>C	XP_005258447.1:n.1266-4G>C
XM_011526265.1:c.1044-4G>C	XP_011524567.1:n.1044-4G>C
XM_011526267.1:c.918-4G>C	XP_011524569.1:n.918-4G>C
XM_011526265.3:c.1044-4G>C	XP_011524567.1:n.1044-4G>C
XM_017026095.1:c.567-4G>C	XP_016881584.1:n.567-4G>C
NM_006033.4:c.1158-4G>C MANE Select	NP_006024.1:n.1158-4G>C
NM_001308006.2:c.936-4G>C	NP_001294935.1:n.936-4G>C