Canonical Allele Identifier: CA1522689899
Gene: LPCAT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1518391A= , CM000667.2:g.1518391A= GRCh38
NC_000005.9:g.1518506A= , CM000667.1:g.1518506A= GRCh37
NC_000005.8:g.1571506A= NCBI36
NG_051622.1:g.10587T=

Transcript Alleles

HGVS Amino-acid change
ENST00000283415.4:c.135+5319T= MANE Select ENSP00000283415.3:n.135+5319T=
ENST00000283415.3:c.135+5319T= ENSP00000283415.3:n.135+5319T=
ENST00000475622.5:c.135+5319T= ENSP00000423472.1:n.135+5319T=
ENST00000514484.6:n.165+2956T=
NM_024830.3:c.135+5319T= NP_079106.3:n.135+5319T=
XM_005248373.2:c.-10+2956T= XP_005248430.1:n.-10+2956T=
XM_011514133.1:c.201+7124T= XP_011512435.1:n.201+7124T=
NM_024830.4:c.135+5319T= NP_079106.3:n.135+5319T=
XM_005248373.3:c.-10+2956T= XP_005248430.1:n.-10+2956T=
NM_024830.5:c.135+5319T= MANE Select NP_079106.3:n.135+5319T=
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