Canonical Allele Identifier: CA544674
Gene: PRDM16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.3425564G>A , CM000663.2:g.3425564G>A GRCh38
NC_000001.10:g.3342128G>A , CM000663.1:g.3342128G>A GRCh37
NC_000001.9:g.3331988G>A NCBI36
NG_029576.1:g.361387G>A
NG_029576.2:g.361387G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270722.10:c.2940-17G>A MANE Select ENSP00000270722.5:n.2940-17G>A
ENST00000270722.9:c.2940-17G>A ENSP00000270722.5:n.2940-17G>A
ENST00000378389.5:n.142-17G>A
ENST00000378391.6:c.2940-17G>A ENSP00000367643.2:n.2940-17G>A
ENST00000509860.1:c.2364-17G>A ENSP00000425796.1:n.2364-17G>A
ENST00000511072.5:c.2943-17G>A ENSP00000426975.1:n.2943-17G>A
ENST00000512462.5:n.2718-17G>A
ENST00000514189.5:c.2940-17G>A ENSP00000421400.1:n.2940-17G>A
ENST00000606170.1:n.349G>A
NM_022114.3:c.2940-17G>A NP_071397.3:n.2940-17G>A
NM_199454.2:c.2940-17G>A NP_955533.2:n.2940-17G>A
XM_005244772.3:c.2943-17G>A XP_005244829.1:n.2943-17G>A
XM_005244773.3:c.2943-17G>A XP_005244830.1:n.2943-17G>A
XM_005244774.3:c.2943-17G>A XP_005244831.1:n.2943-17G>A
XM_006710814.2:c.2940-17G>A XP_006710877.1:n.2940-17G>A
XM_011541944.1:c.2943-17G>A XP_011540246.1:n.2943-17G>A
XM_011541945.1:c.2388-17G>A XP_011540247.1:n.2388-17G>A
XM_005244772.5:c.2943-17G>A XP_005244829.1:n.2943-17G>A
XM_005244773.5:c.2943-17G>A XP_005244830.1:n.2943-17G>A
XM_005244774.5:c.2943-17G>A XP_005244831.1:n.2943-17G>A
XM_006710814.4:c.2940-17G>A XP_006710877.1:n.2940-17G>A
XM_011541945.2:c.2388-17G>A XP_011540247.1:n.2388-17G>A
XM_017002050.1:c.2937-17G>A XP_016857539.1:n.2937-17G>A
NM_022114.4:c.2940-17G>A MANE Select NP_071397.3:n.2940-17G>A
NM_199454.3:c.2940-17G>A NP_955533.2:n.2940-17G>A