Canonical Allele Identifier: CA2635936583

Gene: HES7

Linked Data

• gnomAD v4: 17-8121569-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121569G>T , CM000679.2:g.8121569G>T	GRCh38
NC_000017.10:g.8024887G>T , CM000679.1:g.8024887G>T	GRCh37
NC_000017.9:g.7965612G>T	NCBI36
NG_015807.1:g.2348C>A
NG_015816.1:g.7524C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*2C>A MANE Select	ENSP00000446205.2:n.*2C>A
ENST00000541682.6:c.695C>A	ENSP00000446205.2:n.695C>A
NM_001165967.1:c.*2C>A	NP_001159439.1:n.*2C>A
NM_032580.3:c.*2C>A	NP_115969.2:n.*2C>A
XM_011524038.1:c.*2C>A	XP_011522340.1:n.*2C>A
XM_011524039.1:c.*2C>A	XP_011522341.1:n.*2C>A
XM_011524040.1:c.*2C>A	XP_011522342.1:n.*2C>A
XM_011524041.1:c.*2C>A	XP_011522343.1:n.*2C>A
XM_011524042.1:c.*2C>A	XP_011522344.1:n.*2C>A
XR_934203.1:n.69+1755G>T
XM_017025232.1:c.*2C>A	XP_016880721.1:n.*2C>A
XM_024451007.1:c.*2C>A	XP_024306775.1:n.*2C>A
NM_001165967.2:c.*2C>A MANE Select	NP_001159439.1:n.*2C>A
NM_032580.4:c.*2C>A	NP_115969.2:n.*2C>A