Canonical Allele Identifier: CA1146713577

Gene: PRDM16

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3167258G= , CM000663.2:g.3167258G=	GRCh38
NC_000001.10:g.3083822G= , CM000663.1:g.3083822G=	GRCh37
NC_000001.9:g.3073682G=	NCBI36
NG_029576.1:g.103081G=
NG_029576.2:g.103081G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270722.10:c.38-18867G= MANE Select	ENSP00000270722.5:n.38-18867G=
ENST00000270722.9:c.38-18867G=	ENSP00000270722.5:n.38-18867G=
ENST00000378391.6:c.38-18867G=	ENSP00000367643.2:n.38-18867G=
ENST00000511072.5:c.38-18867G=	ENSP00000426975.1:n.38-18867G=
ENST00000514189.5:c.38-18867G=	ENSP00000421400.1:n.38-18867G=
ENST00000607632.1:n.115-18867G=
NM_022114.3:c.38-18867G=	NP_071397.3:n.38-18867G=
NM_199454.2:c.38-18867G=	NP_955533.2:n.38-18867G=
XM_005244772.3:c.38-18867G=	XP_005244829.1:n.38-18867G=
XM_005244773.3:c.38-18867G=	XP_005244830.1:n.38-18867G=
XM_005244774.3:c.38-18867G=	XP_005244831.1:n.38-18867G=
XM_006710814.2:c.38-18867G=	XP_006710877.1:n.38-18867G=
XM_011541944.1:c.38-18867G=	XP_011540246.1:n.38-18867G=
XR_946881.1:n.316C=
XR_946882.1:n.316C=
XM_005244772.5:c.38-18867G=	XP_005244829.1:n.38-18867G=
XM_005244773.5:c.38-18867G=	XP_005244830.1:n.38-18867G=
XM_005244774.5:c.38-18867G=	XP_005244831.1:n.38-18867G=
XM_006710814.4:c.38-18867G=	XP_006710877.1:n.38-18867G=
XM_017002050.1:c.38-18867G=	XP_016857539.1:n.38-18867G=
XR_001737867.1:n.340C=
NM_022114.4:c.38-18867G= MANE Select	NP_071397.3:n.38-18867G=
NM_199454.3:c.38-18867G=	NP_955533.2:n.38-18867G=