Canonical Allele Identifier: CA397988677

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025268A>C (hg19) ; chr17:g.8121950A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121950A>C , CM000679.2:g.8121950A>C	GRCh38
NC_000017.10:g.8025268A>C , CM000679.1:g.8025268A>C	GRCh37
NC_000017.9:g.7965993A>C	NCBI36
NG_015807.1:g.1967T>G
NG_015816.1:g.7143T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.314T>G MANE Select	ENSP00000446205.2:p.Leu105Arg
ENST00000317814.8:c.299T>G	ENSP00000314774.4:p.Leu100Arg
ENST00000541682.6:c.314T>G	ENSP00000446205.2:p.Leu105Arg
ENST00000577735.1:c.290T>G	ENSP00000462491.1:p.Leu97Arg
NM_001165967.1:c.314T>G	NP_001159439.1:p.Leu105Arg
NM_032580.3:c.299T>G	NP_115969.2:p.Leu100Arg
XM_011524038.1:c.419T>G	XP_011522340.1:p.Leu140Arg
XM_011524039.1:c.410T>G	XP_011522341.1:p.Leu137Arg
XM_011524040.1:c.410T>G	XP_011522342.1:p.Leu137Arg
XM_011524041.1:c.401T>G	XP_011522343.1:p.Leu134Arg
XM_011524042.1:c.272T>G	XP_011522344.1:p.Leu91Arg
XR_934203.1:n.69+2136A>C
XM_017025232.1:c.419T>G	XP_016880721.1:p.Leu140Arg
XM_024451007.1:c.419T>G	XP_024306775.1:p.Leu140Arg
NM_001165967.2:c.314T>G MANE Select	NP_001159439.1:p.Leu105Arg
NM_032580.4:c.299T>G	NP_115969.2:p.Leu100Arg