Canonical Allele Identifier: CA337998935

Gene: PRDM16

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3411952C>G , CM000663.2:g.3411952C>G	GRCh38
NC_000001.10:g.3328516C>G , CM000663.1:g.3328516C>G	GRCh37
NC_000001.9:g.3318376C>G	NCBI36
NG_029576.1:g.347775C>G
NG_029576.2:g.347775C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_022114.4:c.1755C>G MANE Select	NP_071397.3:p.Asp585Glu
ENST00000270722.10:c.1755C>G MANE Select	ENSP00000270722.5:p.Asp585Glu
NM_022114.3:c.1755C>G	NP_071397.3:p.Asp585Glu
NM_199454.2:c.1755C>G	NP_955533.2:p.Asp585Glu
NM_199454.3:c.1755C>G	NP_955533.2:p.Asp585Glu
ENST00000270722.9:c.1755C>G	ENSP00000270722.5:p.Asp585Glu
ENST00000378391.6:c.1755C>G	ENSP00000367643.2:p.Asp585Glu
ENST00000509860.1:c.1182C>G	ENSP00000425796.1:p.Asp394Glu
ENST00000511072.5:c.1758C>G	ENSP00000426975.1:p.Asp586Glu
ENST00000512462.5:n.1533C>G
ENST00000514189.5:c.1758C>G	ENSP00000421400.1:p.Asp586Glu
XM_005244772.3:c.1758C>G	XP_005244829.1:p.Asp586Glu
XM_005244772.5:c.1758C>G	XP_005244829.1:p.Asp586Glu
XM_005244773.3:c.1758C>G	XP_005244830.1:p.Asp586Glu
XM_005244773.5:c.1758C>G	XP_005244830.1:p.Asp586Glu
XM_005244774.3:c.1758C>G	XP_005244831.1:p.Asp586Glu
XM_005244774.5:c.1758C>G	XP_005244831.1:p.Asp586Glu
XM_006710814.2:c.1758C>G	XP_006710877.1:p.Asp586Glu
XM_006710814.4:c.1758C>G	XP_006710877.1:p.Asp586Glu
XM_011541944.1:c.1758C>G	XP_011540246.1:p.Asp586Glu
XM_011541945.1:c.1203C>G	XP_011540247.1:p.Asp401Glu
XM_011541945.2:c.1203C>G	XP_011540247.1:p.Asp401Glu
XM_017002050.1:c.1755C>G	XP_016857539.1:p.Asp585Glu