Canonical Allele Identifier: CA2838198032

Gene: PRDM16

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3138982C>T , CM000663.2:g.3138982C>T	GRCh38
NC_000001.10:g.3055546C>T , CM000663.1:g.3055546C>T	GRCh37
NC_000001.9:g.3045406C>T	NCBI36
NG_029576.1:g.74805C>T
NG_029576.2:g.74805C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270722.10:c.38-47143C>T MANE Select	ENSP00000270722.5:n.38-47143C>T
ENST00000270722.9:c.38-47143C>T	ENSP00000270722.5:n.38-47143C>T
ENST00000378391.6:c.38-47143C>T	ENSP00000367643.2:n.38-47143C>T
ENST00000511072.5:c.38-47143C>T	ENSP00000426975.1:n.38-47143C>T
ENST00000514189.5:c.38-47143C>T	ENSP00000421400.1:n.38-47143C>T
ENST00000607632.1:n.115-47143C>T
NM_022114.3:c.38-47143C>T	NP_071397.3:n.38-47143C>T
NM_199454.2:c.38-47143C>T	NP_955533.2:n.38-47143C>T
XM_005244772.3:c.38-47143C>T	XP_005244829.1:n.38-47143C>T
XM_005244773.3:c.38-47143C>T	XP_005244830.1:n.38-47143C>T
XM_005244774.3:c.38-47143C>T	XP_005244831.1:n.38-47143C>T
XM_006710814.2:c.38-47143C>T	XP_006710877.1:n.38-47143C>T
XM_011541944.1:c.38-47143C>T	XP_011540246.1:n.38-47143C>T
XM_005244772.5:c.38-47143C>T	XP_005244829.1:n.38-47143C>T
XM_005244773.5:c.38-47143C>T	XP_005244830.1:n.38-47143C>T
XM_005244774.5:c.38-47143C>T	XP_005244831.1:n.38-47143C>T
XM_006710814.4:c.38-47143C>T	XP_006710877.1:n.38-47143C>T
XM_017002050.1:c.38-47143C>T	XP_016857539.1:n.38-47143C>T
NM_022114.4:c.38-47143C>T MANE Select	NP_071397.3:n.38-47143C>T
NM_199454.3:c.38-47143C>T	NP_955533.2:n.38-47143C>T