Canonical Allele Identifier: CA805689392

Gene: LPCAT1

Linked Data

• dbSNP Id: rs1171916372
• gnomAD v3: 5-1518290-GCT-G
• gnomAD v4: 5-1518290-GCT-G
• MyVariant Identifiers: chr5:g.1518406_1518407del (hg19) ; chr5:g.1518291_1518292del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1518291_1518292del , CM000667.2:g.1518291_1518292del	GRCh38
NC_000005.9:g.1518406_1518407del , CM000667.1:g.1518406_1518407del	GRCh37
NC_000005.8:g.1571406_1571407del	NCBI36
NG_051622.1:g.10686_10687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283415.4:c.135+5418_135+5419del MANE Select	ENSP00000283415.3:n.135+5418_135+5419del
ENST00000283415.3:c.135+5418_135+5419del	ENSP00000283415.3:n.135+5418_135+5419del
ENST00000475622.5:c.135+5418_135+5419del	ENSP00000423472.1:n.135+5418_135+5419del
ENST00000514484.6:n.165+3055_165+3056del
NM_024830.3:c.135+5418_135+5419del	NP_079106.3:n.135+5418_135+5419del
XM_005248373.2:c.-10+3055_-10+3056del	XP_005248430.1:n.-10+3055_-10+3056del
XM_011514133.1:c.201+7223_201+7224del	XP_011512435.1:n.201+7223_201+7224del
NM_024830.4:c.135+5418_135+5419del	NP_079106.3:n.135+5418_135+5419del
XM_005248373.3:c.-10+3055_-10+3056del	XP_005248430.1:n.-10+3055_-10+3056del
NM_024830.5:c.135+5418_135+5419del MANE Select	NP_079106.3:n.135+5418_135+5419del