Canonical Allele Identifier: CA338003013

Gene: PRDM16

Linked Data

• MyVariant Identifiers: chr1:g.3319376A>T (hg19) ; chr1:g.3402812A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3402812A>T , CM000663.2:g.3402812A>T	GRCh38
NC_000001.10:g.3319376A>T , CM000663.1:g.3319376A>T	GRCh37
NC_000001.9:g.3309236A>T	NCBI36
NG_029576.1:g.338635A>T
NG_029576.2:g.338635A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270722.10:c.698A>T MANE Select	ENSP00000270722.5:p.Asp233Val
ENST00000270722.9:c.698A>T	ENSP00000270722.5:p.Asp233Val
ENST00000378391.6:c.698A>T	ENSP00000367643.2:p.Asp233Val
ENST00000509860.1:c.125A>T	ENSP00000425796.1:p.Asp42Val
ENST00000511072.5:c.701A>T	ENSP00000426975.1:p.Asp234Val
ENST00000512462.5:n.476A>T
ENST00000514189.5:c.701A>T	ENSP00000421400.1:p.Asp234Val
NM_022114.3:c.698A>T	NP_071397.3:p.Asp233Val
NM_199454.2:c.698A>T	NP_955533.2:p.Asp233Val
XM_005244772.3:c.701A>T	XP_005244829.1:p.Asp234Val
XM_005244773.3:c.701A>T	XP_005244830.1:p.Asp234Val
XM_005244774.3:c.701A>T	XP_005244831.1:p.Asp234Val
XM_006710814.2:c.701A>T	XP_006710877.1:p.Asp234Val
XM_011541944.1:c.701A>T	XP_011540246.1:p.Asp234Val
XM_011541945.1:c.146A>T	XP_011540247.1:p.Asp49Val
XM_005244772.5:c.701A>T	XP_005244829.1:p.Asp234Val
XM_005244773.5:c.701A>T	XP_005244830.1:p.Asp234Val
XM_005244774.5:c.701A>T	XP_005244831.1:p.Asp234Val
XM_006710814.4:c.701A>T	XP_006710877.1:p.Asp234Val
XM_011541945.2:c.146A>T	XP_011540247.1:p.Asp49Val
XM_017002050.1:c.698A>T	XP_016857539.1:p.Asp233Val
NM_022114.4:c.698A>T MANE Select	NP_071397.3:p.Asp233Val
NM_199454.3:c.698A>T	NP_955533.2:p.Asp233Val