Canonical Allele Identifier: CA371645317

Gene: GRHL2

Linked Data

• MyVariant Identifiers: chr8:g.102611303T>A (hg19) ; chr8:g.101599075T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101599075T>A , CM000670.2:g.101599075T>A	GRCh38
NC_000008.10:g.102611303T>A , CM000670.1:g.102611303T>A	GRCh37
NC_000008.9:g.102680479T>A	NCBI36
NG_011971.1:g.111636T>A
NG_011971.2:g.111636T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.1022T>A MANE Select	ENSP00000495564.1:p.Phe341Tyr
ENST00000251808.7:c.1022T>A	ENSP00000251808.3:p.Phe341Tyr
ENST00000395927.1:c.974T>A	ENSP00000379260.1:p.Phe325Tyr
NM_024915.3:c.1022T>A	NP_079191.2:p.Phe341Tyr
XM_011517305.1:c.974T>A	XP_011515607.1:p.Phe325Tyr
XM_011517306.1:c.974T>A	XP_011515608.1:p.Phe325Tyr
XM_011517307.1:c.1022T>A	XP_011515609.1:p.Phe341Tyr
NM_001330593.1:c.974T>A	NP_001317522.1:p.Phe325Tyr
XM_011517306.3:c.974T>A	XP_011515608.1:p.Phe325Tyr
XM_011517307.3:c.1022T>A	XP_011515609.1:p.Phe341Tyr
NM_001330593.2:c.974T>A	NP_001317522.1:p.Phe325Tyr
NM_024915.4:c.1022T>A MANE Select	NP_079191.2:p.Phe341Tyr