Canonical Allele Identifier: CA734983018

Gene: PRDM16

Linked Data

• dbSNP Id: rs1253397984
• gnomAD v3: 1-3167241-G-A
• gnomAD v4: 1-3167241-G-A
• MyVariant Identifiers: chr1:g.3083805G>A (hg19) ; chr1:g.3167241G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3167241G>A , CM000663.2:g.3167241G>A	GRCh38
NC_000001.10:g.3083805G>A , CM000663.1:g.3083805G>A	GRCh37
NC_000001.9:g.3073665G>A	NCBI36
NG_029576.1:g.103064G>A
NG_029576.2:g.103064G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000270722.10:c.38-18884G>A MANE Select	ENSP00000270722.5:n.38-18884G>A
ENST00000270722.9:c.38-18884G>A	ENSP00000270722.5:n.38-18884G>A
ENST00000378391.6:c.38-18884G>A	ENSP00000367643.2:n.38-18884G>A
ENST00000511072.5:c.38-18884G>A	ENSP00000426975.1:n.38-18884G>A
ENST00000514189.5:c.38-18884G>A	ENSP00000421400.1:n.38-18884G>A
ENST00000607632.1:n.115-18884G>A
NM_022114.3:c.38-18884G>A	NP_071397.3:n.38-18884G>A
NM_199454.2:c.38-18884G>A	NP_955533.2:n.38-18884G>A
XM_005244772.3:c.38-18884G>A	XP_005244829.1:n.38-18884G>A
XM_005244773.3:c.38-18884G>A	XP_005244830.1:n.38-18884G>A
XM_005244774.3:c.38-18884G>A	XP_005244831.1:n.38-18884G>A
XM_006710814.2:c.38-18884G>A	XP_006710877.1:n.38-18884G>A
XM_011541944.1:c.38-18884G>A	XP_011540246.1:n.38-18884G>A
XR_946881.1:n.333C>T
XR_946882.1:n.333C>T
XM_005244772.5:c.38-18884G>A	XP_005244829.1:n.38-18884G>A
XM_005244773.5:c.38-18884G>A	XP_005244830.1:n.38-18884G>A
XM_005244774.5:c.38-18884G>A	XP_005244831.1:n.38-18884G>A
XM_006710814.4:c.38-18884G>A	XP_006710877.1:n.38-18884G>A
XM_017002050.1:c.38-18884G>A	XP_016857539.1:n.38-18884G>A
XR_001737867.1:n.357C>T
NM_022114.4:c.38-18884G>A MANE Select	NP_071397.3:n.38-18884G>A
NM_199454.3:c.38-18884G>A	NP_955533.2:n.38-18884G>A