Canonical Allele Identifier: CA1522689847
Gene: LPCAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1736567106
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1518295T>A , CM000667.2:g.1518295T>A GRCh38
NC_000005.9:g.1518410T>A , CM000667.1:g.1518410T>A GRCh37
NC_000005.8:g.1571410T>A NCBI36
NG_051622.1:g.10683A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000283415.4:c.135+5415A>T MANE Select ENSP00000283415.3:n.135+5415A>T
ENST00000283415.3:c.135+5415A>T ENSP00000283415.3:n.135+5415A>T
ENST00000475622.5:c.135+5415A>T ENSP00000423472.1:n.135+5415A>T
ENST00000514484.6:n.165+3052A>T
NM_024830.3:c.135+5415A>T NP_079106.3:n.135+5415A>T
XM_005248373.2:c.-10+3052A>T XP_005248430.1:n.-10+3052A>T
XM_011514133.1:c.201+7220A>T XP_011512435.1:n.201+7220A>T
NM_024830.4:c.135+5415A>T NP_079106.3:n.135+5415A>T
XM_005248373.3:c.-10+3052A>T XP_005248430.1:n.-10+3052A>T
NM_024830.5:c.135+5415A>T MANE Select NP_079106.3:n.135+5415A>T
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