Canonical Allele Identifier: CA338215725
Gene: PRDM16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.3186346C>T , CM000663.2:g.3186346C>T GRCh38
NC_000001.10:g.3102910C>T , CM000663.1:g.3102910C>T GRCh37
NC_000001.9:g.3092770C>T NCBI36
NG_029576.1:g.122169C>T
NG_029576.2:g.122169C>T

Transcript Alleles

HGVS Amino-acid Change
NM_022114.4:c.259C>T MANE Select NP_071397.3:p.Arg87Ter
ENST00000270722.10:c.259C>T MANE Select ENSP00000270722.5:p.Arg87Ter
NM_022114.3:c.259C>T NP_071397.3:p.Arg87Ter
NM_199454.2:c.259C>T NP_955533.2:p.Arg87Ter
NM_199454.3:c.259C>T NP_955533.2:p.Arg87Ter
ENST00000270722.9:c.259C>T ENSP00000270722.5:p.Arg87Ter
ENST00000378391.6:c.259C>T ENSP00000367643.2:p.Arg87Ter
ENST00000511072.5:c.259C>T ENSP00000426975.1:p.Arg87Ter
ENST00000514189.5:c.259C>T ENSP00000421400.1:p.Arg87Ter
ENST00000607632.1:n.336C>T
XM_005244772.3:c.259C>T XP_005244829.1:p.Arg87Ter
XM_005244772.5:c.259C>T XP_005244829.1:p.Arg87Ter
XM_005244773.3:c.259C>T XP_005244830.1:p.Arg87Ter
XM_005244773.5:c.259C>T XP_005244830.1:p.Arg87Ter
XM_005244774.3:c.259C>T XP_005244831.1:p.Arg87Ter
XM_005244774.5:c.259C>T XP_005244831.1:p.Arg87Ter
XM_006710814.2:c.259C>T XP_006710877.1:p.Arg87Ter
XM_006710814.4:c.259C>T XP_006710877.1:p.Arg87Ter
XM_011541944.1:c.259C>T XP_011540246.1:p.Arg87Ter
XM_017002050.1:c.259C>T XP_016857539.1:p.Arg87Ter