Canonical Allele Identifier: CA5959881
Community Standard Title: NM_004813.4(PEX16):c.672C>T (p.Tyr224=)
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45914338G>A , CM000673.2:g.45914338G>A GRCh38
NC_000011.9:g.45935889G>A , CM000673.1:g.45935889G>A GRCh37
NC_000011.8:g.45892465G>A NCBI36
NG_008460.1:g.8786C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004813.4:c.672C>T MANE Select NP_004804.2:p.Tyr224=
ENST00000378750.10:c.672C>T MANE Select ENSP00000368024.5:p.Tyr224=
NM_004813.2:c.672C>T NP_004804.1:p.Tyr224=
NM_004813.3:c.672C>T NP_004804.1:p.Tyr224=
NM_057174.2:c.672C>T NP_476515.1:p.Tyr224=
NM_057174.3:c.672C>T NP_476515.2:p.Tyr224=
ENST00000241041.7:c.672C>T ENSP00000241041.3:p.Tyr224=
ENST00000378750.9:c.672C>T ENSP00000368024.5:p.Tyr224=
ENST00000525192.5:c.387C>T ENSP00000431309.1:p.Tyr129=
ENST00000527371.1:n.288C>T
ENST00000532554.5:n.443C>T
ENST00000532681.5:c.387C>T ENSP00000434654.1:p.Tyr129=
ENST00000533151.5:c.360C>T ENSP00000433045.1:p.Tyr120=
XM_011520474.1:c.549C>T XP_011518776.1:p.Tyr183=