Canonical Allele Identifier: CA2809374541

Gene: HNF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37744887_37744888insGGGCGCGGCTAACAAGAGTGCCCA , CM000679.2:g.37744887_37744888insGGGCGCGGCTAACAAGAGTGCCCA	GRCh38
NC_000017.10:g.36104878_36104879insGGGCGCGGCTAACAAGAGTGCCCA , CM000679.1:g.36104878_36104879insGGGCGCGGCTAACAAGAGTGCCCA	GRCh37
NC_000017.9:g.33178991_33178992insGGGCGCGGCTAACAAGAGTGCCCA	NCBI36
NG_013019.2:g.5219_5220insTGGGCACTCTTGTTAGCCGCGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617811.5:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC MANE Select	ENSP00000480291.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
ENST00000613727.4:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	ENSP00000477524.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
ENST00000614313.4:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	ENSP00000482529.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
ENST00000617272.4:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	ENSP00000478682.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
ENST00000617811.4:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	ENSP00000480291.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
ENST00000620125.1:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	ENSP00000481245.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
ENST00000621123.4:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	ENSP00000482711.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
NM_000458.3:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	NP_000449.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
NM_001165923.3:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	NP_001159395.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
NM_001304286.1:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	NP_001291215.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
XM_011525160.1:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	XP_011523462.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
XM_011525161.1:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	XP_011523463.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
XM_011525162.1:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	XP_011523464.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
XM_011525163.1:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	XP_011523465.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
XM_011525164.1:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	XP_011523466.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
XM_011525162.2:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	XP_011523464.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
XM_011525163.2:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	XP_011523465.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
NM_000458.4:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC MANE Select	NP_000449.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
NM_001165923.4:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	NP_001159395.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC
NM_001304286.2:c.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC	NP_001291215.1:n.-4_-3insTGGGCACTCTTGTTAGCCGCGCCC