Canonical Allele Identifier: CA2695225790

Gene: HNF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37739427_37739445del , CM000679.2:g.37739427_37739445del	GRCh38
NC_000017.10:g.36099418_36099436del , CM000679.1:g.36099418_36099436del	GRCh37
NC_000017.9:g.33173531_33173549del	NCBI36
NG_013019.2:g.10665_10683del

Transcript Alleles

HGVS	Amino-acid change
ENST00000617811.5:c.542_544+16del
ENST00000613727.4:c.542_544+16del
ENST00000614313.4:c.542_544+16del
ENST00000617272.4:c.542_544+16del
ENST00000617811.4:c.542_544+16del
ENST00000620125.1:c.542_544+16del
ENST00000621123.4:c.542_544+16del
NM_000458.3:c.542_544+16del
NM_001165923.3:c.542_544+16del
NM_001304286.1:c.542_544+16del
XM_011525160.1:c.542_544+16del
XM_011525161.1:c.542_544+16del
XM_011525162.1:c.542_544+16del
XM_011525163.1:c.542_544+16del
XM_011525164.1:c.542_544+16del
XM_011525162.2:c.542_544+16del
XM_011525163.2:c.542_544+16del
NM_000458.4:c.542_544+16del
NM_001165923.4:c.542_544+16del
NM_001304286.2:c.542_544+16del