Canonical Allele Identifier: CA395196567

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14765138T>G , CM000678.2:g.14765138T>G GRCh38
NC_000016.9:g.14858995T>G , CM000678.1:g.14858995T>G GRCh37
NC_000016.8:g.14766496T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000529166.6:c.835T>G (NPIPA2) MANE Select ENSP00000432029.1:p.Ser279Ala
ENST00000529166.5:c.835T>G (NPIPA2) ENSP00000432029.1:p.Ser279Ala
ENST00000553201.1:c.778T>G (NPIPA2) ENSP00000446882.1:p.Ser260Ala
ENST00000618714.4:c.63+14263T>G (NPIPA1) ENSP00000484994.1:n.63+14263T>G
ENST00000619019.3:c.902-124T>G (NPIPA3) ENSP00000479725.1:n.902-124T>G
ENST00000621766.4:c.778T>G (NPIPA3) ENSP00000483111.1:p.Ser260Ala
NM_001277324.1:c.778T>G (NPIPA2) NP_001264253.1:p.Ser260Ala
XM_005255489.2:c.778T>G (NPIPA2) XP_005255546.1:p.Ser260Ala
XR_933118.1:n.168+1264A>C
XR_933119.1:n.168+1264A>C
XR_933120.1:n.168+1264A>C
XM_024450381.1:c.922T>G (NPIPA2) XP_024306149.1:p.Ser308Ala
XM_024450382.1:c.922T>G (NPIPA2) XP_024306150.1:p.Ser308Ala
XM_024450383.1:c.922T>G (NPIPA2) XP_024306151.1:p.Ser308Ala
XM_024450384.1:c.859T>G (NPIPA2) XP_024306152.1:p.Ser287Ala
XM_024450385.1:c.835T>G (NPIPA2) XP_024306153.1:p.Ser279Ala
XM_024450386.1:c.835T>G (NPIPA2) XP_024306154.1:p.Ser279Ala
XM_024450387.1:c.922T>G (NPIPA2) XP_024306155.1:p.Ser308Ala
XM_024450388.1:c.790T>G (NPIPA2) XP_024306156.1:p.Ser264Ala
XR_933118.2:n.168+1264A>C
XR_933120.2:n.168+1264A>C
NM_001277324.3:c.778T>G (NPIPA2) NP_001264253.1:p.Ser260Ala
NM_001395485.2:c.835T>G (NPIPA2) MANE Select NP_001382414.1:p.Ser279Ala
NM_001395486.2:c.835T>G (NPIPA2) NP_001382415.1:p.Ser279Ala