Canonical Allele Identifier: CA17291124

Gene: PRDM16

Linked Data

• dbSNP Id: rs930173076
• gnomAD v3: 1-3167227-C-T
• gnomAD v4: 1-3167227-C-T
• MyVariant Identifiers: chr1:g.3083791C>T (hg19) ; chr1:g.3167227C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3167227C>T , CM000663.2:g.3167227C>T	GRCh38
NC_000001.10:g.3083791C>T , CM000663.1:g.3083791C>T	GRCh37
NC_000001.9:g.3073651C>T	NCBI36
NG_029576.1:g.103050C>T
NG_029576.2:g.103050C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000270722.10:c.38-18898C>T MANE Select	ENSP00000270722.5:n.38-18898C>T
ENST00000270722.9:c.38-18898C>T	ENSP00000270722.5:n.38-18898C>T
ENST00000378391.6:c.38-18898C>T	ENSP00000367643.2:n.38-18898C>T
ENST00000511072.5:c.38-18898C>T	ENSP00000426975.1:n.38-18898C>T
ENST00000514189.5:c.38-18898C>T	ENSP00000421400.1:n.38-18898C>T
ENST00000607632.1:n.115-18898C>T
NM_022114.3:c.38-18898C>T	NP_071397.3:n.38-18898C>T
NM_199454.2:c.38-18898C>T	NP_955533.2:n.38-18898C>T
XM_005244772.3:c.38-18898C>T	XP_005244829.1:n.38-18898C>T
XM_005244773.3:c.38-18898C>T	XP_005244830.1:n.38-18898C>T
XM_005244774.3:c.38-18898C>T	XP_005244831.1:n.38-18898C>T
XM_006710814.2:c.38-18898C>T	XP_006710877.1:n.38-18898C>T
XM_011541944.1:c.38-18898C>T	XP_011540246.1:n.38-18898C>T
XR_946881.1:n.347G>A
XR_946882.1:n.347G>A
XM_005244772.5:c.38-18898C>T	XP_005244829.1:n.38-18898C>T
XM_005244773.5:c.38-18898C>T	XP_005244830.1:n.38-18898C>T
XM_005244774.5:c.38-18898C>T	XP_005244831.1:n.38-18898C>T
XM_006710814.4:c.38-18898C>T	XP_006710877.1:n.38-18898C>T
XM_017002050.1:c.38-18898C>T	XP_016857539.1:n.38-18898C>T
XR_001737867.1:n.371G>A
NM_022114.4:c.38-18898C>T MANE Select	NP_071397.3:n.38-18898C>T
NM_199454.3:c.38-18898C>T	NP_955533.2:n.38-18898C>T