Canonical Allele Identifier: CA2838251109

Gene: ZBTB48

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6581311A>G , CM000663.2:g.6581311A>G	GRCh38
NC_000001.10:g.6641371A>G , CM000663.1:g.6641371A>G	GRCh37
NC_000001.9:g.6563958A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377674.9:c.690+12A>G MANE Select	ENSP00000366902.4:n.690+12A>G
ENST00000319084.9:c.690+12A>G	ENSP00000313416.5:n.690+12A>G
ENST00000377674.8:c.690+12A>G	ENSP00000366902.4:n.690+12A>G
ENST00000435905.5:c.690+12A>G	ENSP00000416054.1:n.690+12A>G
ENST00000488936.1:c.-45-747A>G	ENSP00000466390.1:n.-45-747A>G
NM_001278647.1:c.690+12A>G	NP_001265576.1:n.690+12A>G
NM_001278648.1:c.690+12A>G	NP_001265577.1:n.690+12A>G
NM_005341.3:c.690+12A>G	NP_005332.1:n.690+12A>G
XM_011541310.1:c.5+12A>G	XP_011539612.1:n.5+12A>G
XR_946621.1:n.874+12A>G
XR_946622.1:n.876+12A>G
XR_946623.1:n.875+12A>G
XM_017001110.2:c.690+12A>G	XP_016856599.1:n.690+12A>G
XM_017001111.2:c.690+12A>G	XP_016856600.1:n.690+12A>G
XM_017001112.2:c.-497+12A>G	XP_016856601.1:n.-497+12A>G
XM_017001113.2:c.-497+12A>G	XP_016856602.1:n.-497+12A>G
XM_017001114.2:c.-285+12A>G	XP_016856603.1:n.-285+12A>G
XR_001737135.2:n.836+12A>G
XR_001737136.1:n.815+12A>G
XR_001737137.2:n.781+12A>G
XR_946621.3:n.781+12A>G
NM_005341.4:c.690+12A>G MANE Select	NP_005332.1:n.690+12A>G
NM_001278647.2:c.690+12A>G	NP_001265576.1:n.690+12A>G
NM_001278648.2:c.690+12A>G	NP_001265577.1:n.690+12A>G