Canonical Allele Identifier: CA1806421545

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101644170_101644173delinsAGAG , CM000670.2:g.101644170_101644173delinsAGAG	GRCh38
NC_000008.10:g.102656398_102656401delinsAGAG , CM000670.1:g.102656398_102656401delinsAGAG	GRCh37
NC_000008.9:g.102725574_102725577delinsAGAG	NCBI36
NG_011971.1:g.156731_156734delinsAGAG
NG_011971.2:g.156731_156734delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.1557_1560delinsAGAG MANE Select	ENSP00000495564.1:p.Glu519=
ENST00000251808.7:c.1557_1560delinsAGAG	ENSP00000251808.3:p.Glu519=
ENST00000395927.1:c.1509_1512delinsAGAG	ENSP00000379260.1:p.Glu503=
ENST00000474338.1:n.199_202delinsAGAG
ENST00000517674.5:n.212_215delinsAGAG
NM_024915.3:c.1557_1560delinsAGAG	NP_079191.2:p.Glu519=
XM_011517305.1:c.1509_1512delinsAGAG	XP_011515607.1:p.Glu503=
XM_011517306.1:c.1509_1512delinsAGAG	XP_011515608.1:p.Glu503=
XM_011517307.1:c.1557_1560delinsAGAG	XP_011515609.1:p.Glu519=
NM_001330593.1:c.1509_1512delinsAGAG	NP_001317522.1:p.Glu503=
XM_011517306.3:c.1509_1512delinsAGAG	XP_011515608.1:p.Glu503=
XM_011517307.3:c.1557_1560delinsAGAG	XP_011515609.1:p.Glu519=
NM_001330593.2:c.1509_1512delinsAGAG	NP_001317522.1:p.Glu503=
NM_024915.4:c.1557_1560delinsAGAG MANE Select	NP_079191.2:p.Glu519=