Canonical Allele Identifier: CA112991424

Gene: LPCAT1

Linked Data

• dbSNP Id: rs139852726
• gnomAD v3: 5-1462734-G-A
• gnomAD v4: 5-1462734-G-A
• MyVariant Identifiers: chr5:g.1462849G>A (hg19) ; chr5:g.1462734G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1462734G>A , CM000667.2:g.1462734G>A	GRCh38
NC_000005.9:g.1462849G>A , CM000667.1:g.1462849G>A	GRCh37
NC_000005.8:g.1515849G>A	NCBI36
NG_051622.1:g.66244C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000283415.4:c.*917C>T MANE Select	ENSP00000283415.3:n.*917C>T
ENST00000283415.3:c.*917C>T	ENSP00000283415.3:n.*917C>T
ENST00000475622.5:c.*917C>T	ENSP00000423472.1:n.*917C>T
ENST00000503252.1:n.1389C>T
NM_024830.3:c.*917C>T	NP_079106.3:n.*917C>T
XM_005248373.2:c.*917C>T	XP_005248430.1:n.*917C>T
XM_011514132.1:c.*917C>T	XP_011512434.1:n.*917C>T
XM_011514133.1:c.*917C>T	XP_011512435.1:n.*917C>T
XM_011514134.1:c.*917C>T	XP_011512436.1:n.*917C>T
NM_024830.4:c.*917C>T	NP_079106.3:n.*917C>T
XM_005248373.3:c.*917C>T	XP_005248430.1:n.*917C>T
XM_017009879.2:c.*917C>T	XP_016865368.1:n.*917C>T
NM_024830.5:c.*917C>T MANE Select	NP_079106.3:n.*917C>T