Canonical Allele Identifier: CA7584927
Community Standard Title: NM_000236.3(LIPC):c.575-15C>T
Gene: LIPC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58545727C>T , CM000677.2:g.58545727C>T GRCh38
NC_000015.9:g.58837926C>T , CM000677.1:g.58837926C>T GRCh37
NC_000015.8:g.56625218C>T NCBI36
NG_011465.1:g.118752C>T
NG_011465.2:g.118752C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000236.3:c.575-15C>T MANE Select NP_000227.2:n.575-15C>T
ENST00000299022.10:c.575-15C>T MANE Select ENSP00000299022.5:n.575-15C>T
NM_000236.2:c.575-15C>T NP_000227.2:n.575-15C>T
ENST00000299022.9:c.575-15C>T ENSP00000299022.5:n.575-15C>T
ENST00000356113.10:c.575-15C>T ENSP00000348425.6:n.575-15C>T
ENST00000414170.7:c.575-15C>T ENSP00000395569.3:n.575-15C>T
ENST00000433326.2:c.392-15C>T ENSP00000395002.2:n.392-15C>T
ENST00000559845.5:n.432-15C>T
ENST00000560664.1:n.339-15C>T
XM_005254372.1:c.575-15C>T XP_005254429.1:n.575-15C>T
XM_005254374.3:c.512-15C>T XP_005254431.1:n.512-15C>T
XM_005254374.4:c.611-15C>T XP_005254431.2:n.611-15C>T
XM_006720502.2:c.434-15C>T XP_006720565.1:n.434-15C>T
XM_006720502.4:c.434-15C>T XP_006720565.1:n.434-15C>T
XM_011521551.1:c.575-15C>T XP_011519853.1:n.575-15C>T
XM_017022176.1:c.611-15C>T XP_016877665.1:n.611-15C>T
XM_024449916.1:c.575-15C>T XP_024305684.1:n.575-15C>T
XM_024449917.1:c.575-15C>T XP_024305685.1:n.575-15C>T