Canonical Allele Identifier: CA15921418

Gene: LIPG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49583323G>A , CM000680.2:g.49583323G>A	GRCh38
NC_000018.9:g.47109693G>A , CM000680.1:g.47109693G>A	GRCh37
NC_000018.8:g.45363691G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261292.9:c.1158-233G>A MANE Select	ENSP00000261292.4:n.1158-233G>A
ENST00000261292.8:c.1158-233G>A	ENSP00000261292.4:n.1158-233G>A
ENST00000427224.6:c.936-233G>A	ENSP00000387978.2:n.936-233G>A
NM_001308006.1:c.936-233G>A	NP_001294935.1:n.936-233G>A
NM_006033.2:c.1158-233G>A	NP_006024.1:n.1158-233G>A
NM_006033.3:c.1158-233G>A	NP_006024.1:n.1158-233G>A
XM_005258390.1:c.1266-233G>A	XP_005258447.1:n.1266-233G>A
XM_011526265.1:c.1044-233G>A	XP_011524567.1:n.1044-233G>A
XM_011526267.1:c.918-233G>A	XP_011524569.1:n.918-233G>A
XM_011526265.3:c.1044-233G>A	XP_011524567.1:n.1044-233G>A
XM_017026095.1:c.567-233G>A	XP_016881584.1:n.567-233G>A
NM_006033.4:c.1158-233G>A MANE Select	NP_006024.1:n.1158-233G>A
NM_001308006.2:c.936-233G>A	NP_001294935.1:n.936-233G>A