Canonical Allele Identifier: CA1149997415

Gene: PRDM16

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3167004_3167005delinsCG , CM000663.2:g.3167004_3167005delinsCG	GRCh38
NC_000001.10:g.3083568_3083569delinsCG , CM000663.1:g.3083568_3083569delinsCG	GRCh37
NC_000001.9:g.3073428_3073429delinsCG	NCBI36
NG_029576.1:g.102827_102828delinsCG
NG_029576.2:g.102827_102828delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000270722.10:c.38-19121_38-19120delinsCG MANE Select	ENSP00000270722.5:n.38-19121_38-19120delinsCG
ENST00000270722.9:c.38-19121_38-19120delinsCG	ENSP00000270722.5:n.38-19121_38-19120delinsCG
ENST00000378391.6:c.38-19121_38-19120delinsCG	ENSP00000367643.2:n.38-19121_38-19120delinsCG
ENST00000511072.5:c.38-19121_38-19120delinsCG	ENSP00000426975.1:n.38-19121_38-19120delinsCG
ENST00000514189.5:c.38-19121_38-19120delinsCG	ENSP00000421400.1:n.38-19121_38-19120delinsCG
ENST00000607632.1:n.115-19121_115-19120delinsCG
NM_022114.3:c.38-19121_38-19120delinsCG	NP_071397.3:n.38-19121_38-19120delinsCG
NM_199454.2:c.38-19121_38-19120delinsCG	NP_955533.2:n.38-19121_38-19120delinsCG
XM_005244772.3:c.38-19121_38-19120delinsCG	XP_005244829.1:n.38-19121_38-19120delinsCG
XM_005244773.3:c.38-19121_38-19120delinsCG	XP_005244830.1:n.38-19121_38-19120delinsCG
XM_005244774.3:c.38-19121_38-19120delinsCG	XP_005244831.1:n.38-19121_38-19120delinsCG
XM_006710814.2:c.38-19121_38-19120delinsCG	XP_006710877.1:n.38-19121_38-19120delinsCG
XM_011541944.1:c.38-19121_38-19120delinsCG	XP_011540246.1:n.38-19121_38-19120delinsCG
XR_946881.1:n.569_570delinsCG
XR_946882.1:n.569_570delinsCG
XM_005244772.5:c.38-19121_38-19120delinsCG	XP_005244829.1:n.38-19121_38-19120delinsCG
XM_005244773.5:c.38-19121_38-19120delinsCG	XP_005244830.1:n.38-19121_38-19120delinsCG
XM_005244774.5:c.38-19121_38-19120delinsCG	XP_005244831.1:n.38-19121_38-19120delinsCG
XM_006710814.4:c.38-19121_38-19120delinsCG	XP_006710877.1:n.38-19121_38-19120delinsCG
XM_017002050.1:c.38-19121_38-19120delinsCG	XP_016857539.1:n.38-19121_38-19120delinsCG
XR_001737867.1:n.593_594delinsCG
NM_022114.4:c.38-19121_38-19120delinsCG MANE Select	NP_071397.3:n.38-19121_38-19120delinsCG
NM_199454.3:c.38-19121_38-19120delinsCG	NP_955533.2:n.38-19121_38-19120delinsCG