Canonical Allele Identifier: CA394662878
Gene: NAGPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5028972T>A , CM000678.2:g.5028972T>A GRCh38
NC_000016.9:g.5078973T>A , CM000678.1:g.5078973T>A GRCh37
NC_000016.8:g.5018974T>A NCBI36
NG_028152.1:g.9970A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000312251.8:c.828A>T MANE Select ENSP00000310998.3:p.Lys276Asn
ENST00000649828.1:c.828A>T ENSP00000498032.1:p.Lys276Asn
ENST00000312251.7:c.828A>T ENSP00000310998.3:p.Lys276Asn
ENST00000381955.7:c.828A>T ENSP00000371381.3:p.Lys276Asn
ENST00000562037.1:c.589A>T ENSP00000464994.1:n.589A>T
ENST00000562346.2:c.505-787A>T
ENST00000562746.5:c.828A>T ENSP00000455900.1:p.Lys276Asn
ENST00000563578.5:c.646A>T
ENST00000564397.5:n.1187A>T
ENST00000565876.5:c.480+1413A>T
ENST00000567739.5:n.147A>T
ENST00000568202.5:n.691A>T
ENST00000569296.5:c.372A>T ENSP00000465949.1:p.Lys124Asn
NM_016256.3:c.828A>T NP_057340.2:p.Lys276Asn
XM_011522517.1:c.828A>T XP_011520819.1:p.Lys276Asn
XM_011522518.1:c.828A>T XP_011520820.1:p.Lys276Asn
XM_011522519.1:c.828A>T XP_011520821.1:p.Lys276Asn
XR_243285.1:n.855A>T
XM_011522517.3:c.828A>T XP_011520819.1:p.Lys276Asn
XR_001751908.2:n.854A>T
XR_001751909.2:n.854A>T
XR_001751910.2:n.854A>T
XR_001751911.2:n.854A>T
XR_001751912.2:n.854A>T
NM_016256.4:c.828A>T MANE Select NP_057340.2:p.Lys276Asn