Canonical Allele Identifier: CA338002984

Gene: PRDM16

Linked Data

• MyVariant Identifiers: chr1:g.3319363A>G (hg19) ; chr1:g.3402799A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3402799A>G , CM000663.2:g.3402799A>G	GRCh38
NC_000001.10:g.3319363A>G , CM000663.1:g.3319363A>G	GRCh37
NC_000001.9:g.3309223A>G	NCBI36
NG_029576.1:g.338622A>G
NG_029576.2:g.338622A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270722.10:c.685A>G MANE Select	ENSP00000270722.5:p.Thr229Ala
ENST00000270722.9:c.685A>G	ENSP00000270722.5:p.Thr229Ala
ENST00000378391.6:c.685A>G	ENSP00000367643.2:p.Thr229Ala
ENST00000509860.1:c.112A>G	ENSP00000425796.1:p.Thr38Ala
ENST00000511072.5:c.688A>G	ENSP00000426975.1:p.Thr230Ala
ENST00000512462.5:n.463A>G
ENST00000514189.5:c.688A>G	ENSP00000421400.1:p.Thr230Ala
NM_022114.3:c.685A>G	NP_071397.3:p.Thr229Ala
NM_199454.2:c.685A>G	NP_955533.2:p.Thr229Ala
XM_005244772.3:c.688A>G	XP_005244829.1:p.Thr230Ala
XM_005244773.3:c.688A>G	XP_005244830.1:p.Thr230Ala
XM_005244774.3:c.688A>G	XP_005244831.1:p.Thr230Ala
XM_006710814.2:c.688A>G	XP_006710877.1:p.Thr230Ala
XM_011541944.1:c.688A>G	XP_011540246.1:p.Thr230Ala
XM_011541945.1:c.133A>G	XP_011540247.1:p.Thr45Ala
XM_005244772.5:c.688A>G	XP_005244829.1:p.Thr230Ala
XM_005244773.5:c.688A>G	XP_005244830.1:p.Thr230Ala
XM_005244774.5:c.688A>G	XP_005244831.1:p.Thr230Ala
XM_006710814.4:c.688A>G	XP_006710877.1:p.Thr230Ala
XM_011541945.2:c.133A>G	XP_011540247.1:p.Thr45Ala
XM_017002050.1:c.685A>G	XP_016857539.1:p.Thr229Ala
NM_022114.4:c.685A>G MANE Select	NP_071397.3:p.Thr229Ala
NM_199454.3:c.685A>G	NP_955533.2:p.Thr229Ala