Canonical Allele Identifier: CA2246159731

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121558_8121559delinsCA , CM000679.2:g.8121558_8121559delinsCA	GRCh38
NC_000017.10:g.8024876_8024877delinsCA , CM000679.1:g.8024876_8024877delinsCA	GRCh37
NC_000017.9:g.7965601_7965602delinsCA	NCBI36
NG_015807.1:g.2358_2359delinsTG
NG_015816.1:g.7534_7535delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*12_*13delinsTG MANE Select	ENSP00000446205.2:n.*12_*13delinsTG
ENST00000541682.6:c.705_706delinsTG	ENSP00000446205.2:n.705_706delinsTG
NM_001165967.1:c.*12_*13delinsTG	NP_001159439.1:n.*12_*13delinsTG
NM_032580.3:c.*12_*13delinsTG	NP_115969.2:n.*12_*13delinsTG
XM_011524038.1:c.*12_*13delinsTG	XP_011522340.1:n.*12_*13delinsTG
XM_011524039.1:c.*12_*13delinsTG	XP_011522341.1:n.*12_*13delinsTG
XM_011524040.1:c.*12_*13delinsTG	XP_011522342.1:n.*12_*13delinsTG
XM_011524041.1:c.*12_*13delinsTG	XP_011522343.1:n.*12_*13delinsTG
XM_011524042.1:c.*12_*13delinsTG	XP_011522344.1:n.*12_*13delinsTG
XR_934203.1:n.69+1744_69+1745delinsCA
XM_017025232.1:c.*12_*13delinsTG	XP_016880721.1:n.*12_*13delinsTG
XM_024451007.1:c.*12_*13delinsTG	XP_024306775.1:n.*12_*13delinsTG
NM_001165967.2:c.*12_*13delinsTG MANE Select	NP_001159439.1:n.*12_*13delinsTG
NM_032580.4:c.*12_*13delinsTG	NP_115969.2:n.*12_*13delinsTG