Canonical Allele Identifier: CA299941255

Gene: LIPG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49583457C>T , CM000680.2:g.49583457C>T	GRCh38
NC_000018.9:g.47109827C>T , CM000680.1:g.47109827C>T	GRCh37
NC_000018.8:g.45363825C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006033.4:c.1158-99C>T MANE Select	NP_006024.1:n.1158-99C>T
ENST00000261292.9:c.1158-99C>T MANE Select	ENSP00000261292.4:n.1158-99C>T
NM_001308006.1:c.936-99C>T	NP_001294935.1:n.936-99C>T
NM_001308006.2:c.936-99C>T	NP_001294935.1:n.936-99C>T
NM_006033.2:c.1158-99C>T	NP_006024.1:n.1158-99C>T
NM_006033.3:c.1158-99C>T	NP_006024.1:n.1158-99C>T
ENST00000261292.8:c.1158-99C>T	ENSP00000261292.4:n.1158-99C>T
ENST00000427224.6:c.936-99C>T	ENSP00000387978.2:n.936-99C>T
XM_005258390.1:c.1266-99C>T	XP_005258447.1:n.1266-99C>T
XM_011526265.1:c.1044-99C>T	XP_011524567.1:n.1044-99C>T
XM_011526265.3:c.1044-99C>T	XP_011524567.1:n.1044-99C>T
XM_011526267.1:c.918-99C>T	XP_011524569.1:n.918-99C>T
XM_017026095.1:c.567-99C>T	XP_016881584.1:n.567-99C>T