Canonical Allele Identifier: CA17291120

Gene: PRDM16

Linked Data

• dbSNP Id: rs111818048
• MyVariant Identifiers: chr1:g.3083748A>G (hg19) ; chr1:g.3167184A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3167184A>G , CM000663.2:g.3167184A>G	GRCh38
NC_000001.10:g.3083748A>G , CM000663.1:g.3083748A>G	GRCh37
NC_000001.9:g.3073608A>G	NCBI36
NG_029576.1:g.103007A>G
NG_029576.2:g.103007A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000270722.10:c.38-18941A>G MANE Select	ENSP00000270722.5:n.38-18941A>G
ENST00000270722.9:c.38-18941A>G	ENSP00000270722.5:n.38-18941A>G
ENST00000378391.6:c.38-18941A>G	ENSP00000367643.2:n.38-18941A>G
ENST00000511072.5:c.38-18941A>G	ENSP00000426975.1:n.38-18941A>G
ENST00000514189.5:c.38-18941A>G	ENSP00000421400.1:n.38-18941A>G
ENST00000607632.1:n.115-18941A>G
NM_022114.3:c.38-18941A>G	NP_071397.3:n.38-18941A>G
NM_199454.2:c.38-18941A>G	NP_955533.2:n.38-18941A>G
XM_005244772.3:c.38-18941A>G	XP_005244829.1:n.38-18941A>G
XM_005244773.3:c.38-18941A>G	XP_005244830.1:n.38-18941A>G
XM_005244774.3:c.38-18941A>G	XP_005244831.1:n.38-18941A>G
XM_006710814.2:c.38-18941A>G	XP_006710877.1:n.38-18941A>G
XM_011541944.1:c.38-18941A>G	XP_011540246.1:n.38-18941A>G
XR_946881.1:n.390T>C
XR_946882.1:n.390T>C
XM_005244772.5:c.38-18941A>G	XP_005244829.1:n.38-18941A>G
XM_005244773.5:c.38-18941A>G	XP_005244830.1:n.38-18941A>G
XM_005244774.5:c.38-18941A>G	XP_005244831.1:n.38-18941A>G
XM_006710814.4:c.38-18941A>G	XP_006710877.1:n.38-18941A>G
XM_017002050.1:c.38-18941A>G	XP_016857539.1:n.38-18941A>G
XR_001737867.1:n.414T>C
NM_022114.4:c.38-18941A>G MANE Select	NP_071397.3:n.38-18941A>G
NM_199454.3:c.38-18941A>G	NP_955533.2:n.38-18941A>G