Canonical Allele Identifier: CA1522689848
Gene: LPCAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1736567106
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Genomic Alleles

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

Transcript Alleles

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