Canonical Allele Identifier: CA2246159700

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121541_8121542delinsCT , CM000679.2:g.8121541_8121542delinsCT	GRCh38
NC_000017.10:g.8024859_8024860delinsCT , CM000679.1:g.8024859_8024860delinsCT	GRCh37
NC_000017.9:g.7965584_7965585delinsCT	NCBI36
NG_015807.1:g.2375_2376delinsAG
NG_015816.1:g.7551_7552delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*29_*30delinsAG MANE Select	ENSP00000446205.2:n.*29_*30delinsAG
ENST00000541682.6:c.722_723delinsAG	ENSP00000446205.2:n.722_723delinsAG
NM_001165967.1:c.*29_*30delinsAG	NP_001159439.1:n.*29_*30delinsAG
NM_032580.3:c.*29_*30delinsAG	NP_115969.2:n.*29_*30delinsAG
XM_011524038.1:c.*29_*30delinsAG	XP_011522340.1:n.*29_*30delinsAG
XM_011524039.1:c.*29_*30delinsAG	XP_011522341.1:n.*29_*30delinsAG
XM_011524040.1:c.*29_*30delinsAG	XP_011522342.1:n.*29_*30delinsAG
XM_011524041.1:c.*29_*30delinsAG	XP_011522343.1:n.*29_*30delinsAG
XM_011524042.1:c.*29_*30delinsAG	XP_011522344.1:n.*29_*30delinsAG
XR_934203.1:n.69+1727_69+1728delinsCT
XM_017025232.1:c.*29_*30delinsAG	XP_016880721.1:n.*29_*30delinsAG
XM_024451007.1:c.*29_*30delinsAG	XP_024306775.1:n.*29_*30delinsAG
NM_001165967.2:c.*29_*30delinsAG MANE Select	NP_001159439.1:n.*29_*30delinsAG
NM_032580.4:c.*29_*30delinsAG	NP_115969.2:n.*29_*30delinsAG