Canonical Allele Identifier: CA14517121

Gene: LIPG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49569117T>C , CM000680.2:g.49569117T>C	GRCh38
NC_000018.9:g.47095487T>C , CM000680.1:g.47095487T>C	GRCh37
NC_000018.8:g.45349485T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006033.4:c.460-320T>C MANE Select	NP_006024.1:n.460-320T>C
ENST00000261292.9:c.460-320T>C MANE Select	ENSP00000261292.4:n.460-320T>C
NM_001308006.1:c.460-320T>C	NP_001294935.1:n.460-320T>C
NM_001308006.2:c.460-320T>C	NP_001294935.1:n.460-320T>C
NM_006033.2:c.460-320T>C	NP_006024.1:n.460-320T>C
NM_006033.3:c.460-320T>C	NP_006024.1:n.460-320T>C
ENST00000261292.8:c.460-320T>C	ENSP00000261292.4:n.460-320T>C
ENST00000427224.6:c.460-320T>C	ENSP00000387978.2:n.460-320T>C
ENST00000577628.5:c.568-320T>C	ENSP00000463835.1:n.568-320T>C
ENST00000580036.5:c.460-320T>C	ENSP00000462420.1:n.460-320T>C
XM_005258390.1:c.568-320T>C	XP_005258447.1:n.568-320T>C
XM_011526265.1:c.568-320T>C	XP_011524567.1:n.568-320T>C
XM_011526265.3:c.568-320T>C	XP_011524567.1:n.568-320T>C
XM_011526267.1:c.220-320T>C	XP_011524569.1:n.220-320T>C
XM_017026095.1:c.-244-320T>C	XP_016881584.1:n.-244-320T>C