Canonical Allele Identifier: CA1149997866

Gene: PRDM16

Linked Data

• dbSNP Id: rs570587337

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3167270G>C , CM000663.2:g.3167270G>C	GRCh38
NC_000001.10:g.3083834G>C , CM000663.1:g.3083834G>C	GRCh37
NC_000001.9:g.3073694G>C	NCBI36
NG_029576.1:g.103093G>C
NG_029576.2:g.103093G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270722.10:c.38-18855G>C MANE Select	ENSP00000270722.5:n.38-18855G>C
ENST00000270722.9:c.38-18855G>C	ENSP00000270722.5:n.38-18855G>C
ENST00000378391.6:c.38-18855G>C	ENSP00000367643.2:n.38-18855G>C
ENST00000511072.5:c.38-18855G>C	ENSP00000426975.1:n.38-18855G>C
ENST00000514189.5:c.38-18855G>C	ENSP00000421400.1:n.38-18855G>C
ENST00000607632.1:n.115-18855G>C
NM_022114.3:c.38-18855G>C	NP_071397.3:n.38-18855G>C
NM_199454.2:c.38-18855G>C	NP_955533.2:n.38-18855G>C
XM_005244772.3:c.38-18855G>C	XP_005244829.1:n.38-18855G>C
XM_005244773.3:c.38-18855G>C	XP_005244830.1:n.38-18855G>C
XM_005244774.3:c.38-18855G>C	XP_005244831.1:n.38-18855G>C
XM_006710814.2:c.38-18855G>C	XP_006710877.1:n.38-18855G>C
XM_011541944.1:c.38-18855G>C	XP_011540246.1:n.38-18855G>C
XR_946881.1:n.304C>G
XR_946882.1:n.304C>G
XM_005244772.5:c.38-18855G>C	XP_005244829.1:n.38-18855G>C
XM_005244773.5:c.38-18855G>C	XP_005244830.1:n.38-18855G>C
XM_005244774.5:c.38-18855G>C	XP_005244831.1:n.38-18855G>C
XM_006710814.4:c.38-18855G>C	XP_006710877.1:n.38-18855G>C
XM_017002050.1:c.38-18855G>C	XP_016857539.1:n.38-18855G>C
XR_001737867.1:n.328C>G
NM_022114.4:c.38-18855G>C MANE Select	NP_071397.3:n.38-18855G>C
NM_199454.3:c.38-18855G>C	NP_955533.2:n.38-18855G>C