Canonical Allele Identifier: CA557565643

Gene: LPCAT1

Linked Data

• dbSNP Id: rs924092552
• gnomAD v2: 5-1518396-T-C
• gnomAD v3: 5-1518281-T-C
• gnomAD v4: 5-1518281-T-C
• MyVariant Identifiers: chr5:g.1518396T>C (hg19) ; chr5:g.1518281T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1518281T>C , CM000667.2:g.1518281T>C	GRCh38
NC_000005.9:g.1518396T>C , CM000667.1:g.1518396T>C	GRCh37
NC_000005.8:g.1571396T>C	NCBI36
NG_051622.1:g.10697A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283415.4:c.135+5429A>G MANE Select	ENSP00000283415.3:n.135+5429A>G
ENST00000283415.3:c.135+5429A>G	ENSP00000283415.3:n.135+5429A>G
ENST00000475622.5:c.135+5429A>G	ENSP00000423472.1:n.135+5429A>G
ENST00000514484.6:n.165+3066A>G
NM_024830.3:c.135+5429A>G	NP_079106.3:n.135+5429A>G
XM_005248373.2:c.-10+3066A>G	XP_005248430.1:n.-10+3066A>G
XM_011514133.1:c.201+7234A>G	XP_011512435.1:n.201+7234A>G
NM_024830.4:c.135+5429A>G	NP_079106.3:n.135+5429A>G
XM_005248373.3:c.-10+3066A>G	XP_005248430.1:n.-10+3066A>G
NM_024830.5:c.135+5429A>G MANE Select	NP_079106.3:n.135+5429A>G