Canonical Allele Identifier: CA1522689844
Gene: LPCAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1736567039
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1518294A>T , CM000667.2:g.1518294A>T GRCh38
NC_000005.9:g.1518409A>T , CM000667.1:g.1518409A>T GRCh37
NC_000005.8:g.1571409A>T NCBI36
NG_051622.1:g.10684T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000283415.4:c.135+5416T>A MANE Select ENSP00000283415.3:n.135+5416T>A
ENST00000283415.3:c.135+5416T>A ENSP00000283415.3:n.135+5416T>A
ENST00000475622.5:c.135+5416T>A ENSP00000423472.1:n.135+5416T>A
ENST00000514484.6:n.165+3053T>A
NM_024830.3:c.135+5416T>A NP_079106.3:n.135+5416T>A
XM_005248373.2:c.-10+3053T>A XP_005248430.1:n.-10+3053T>A
XM_011514133.1:c.201+7221T>A XP_011512435.1:n.201+7221T>A
NM_024830.4:c.135+5416T>A NP_079106.3:n.135+5416T>A
XM_005248373.3:c.-10+3053T>A XP_005248430.1:n.-10+3053T>A
NM_024830.5:c.135+5416T>A MANE Select NP_079106.3:n.135+5416T>A
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