Canonical Allele Identifier: CA1522689851
Gene: LPCAT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1518309T= , CM000667.2:g.1518309T= GRCh38
NC_000005.9:g.1518424T= , CM000667.1:g.1518424T= GRCh37
NC_000005.8:g.1571424T= NCBI36
NG_051622.1:g.10669A=

Transcript Alleles

HGVS Amino-acid change
ENST00000283415.4:c.135+5401A= MANE Select ENSP00000283415.3:n.135+5401A=
ENST00000283415.3:c.135+5401A= ENSP00000283415.3:n.135+5401A=
ENST00000475622.5:c.135+5401A= ENSP00000423472.1:n.135+5401A=
ENST00000514484.6:n.165+3038A=
NM_024830.3:c.135+5401A= NP_079106.3:n.135+5401A=
XM_005248373.2:c.-10+3038A= XP_005248430.1:n.-10+3038A=
XM_011514133.1:c.201+7206A= XP_011512435.1:n.201+7206A=
NM_024830.4:c.135+5401A= NP_079106.3:n.135+5401A=
XM_005248373.3:c.-10+3038A= XP_005248430.1:n.-10+3038A=
NM_024830.5:c.135+5401A= MANE Select NP_079106.3:n.135+5401A=
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