Canonical Allele Identifier: CA689818

Gene: GRHL3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.24331582G>A , CM000663.2:g.24331582G>A	GRCh38
NC_000001.10:g.24658072G>A , CM000663.1:g.24658072G>A	GRCh37
NC_000001.9:g.24530659G>A	NCBI36
NG_009308.1:g.17192G>A
NG_009308.2:g.17192G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461318.2:c.174G>A	ENSP00000508789.1:p.Ala58=
ENST00000524724.6:c.36G>A	ENSP00000431290.2:p.Ala12=
ENST00000528064.6:c.-75-3063G>A	ENSP00000435130.2:n.-75-3063G>A
ENST00000689444.1:c.36G>A	ENSP00000509040.1:p.Ala12=
ENST00000690803.1:c.-75-3063G>A	ENSP00000510783.1:n.-75-3063G>A
ENST00000692334.1:c.-75-3063G>A	ENSP00000509790.1:n.-75-3063G>A
ENST00000361548.9:c.174G>A MANE Select	ENSP00000354943.5:p.Ala58=
ENST00000236255.4:c.189G>A	ENSP00000236255.4:p.Ala63=
ENST00000350501.9:c.174G>A	ENSP00000288955.5:p.Ala58=
ENST00000356046.6:c.36G>A	ENSP00000348333.2:p.Ala12=
ENST00000361548.8:c.174G>A	ENSP00000354943.4:p.Ala58=
ENST00000524724.5:c.36G>A	ENSP00000431290.1:p.Ala12=
ENST00000528064.5:c.33-3063G>A	ENSP00000435130.1:n.33-3063G>A
ENST00000530984.1:n.270G>A
NM_001195010.1:c.36G>A	NP_001181939.1:p.Ala12=
NM_021180.3:c.189G>A	NP_067003.2:p.Ala63=
NM_198173.2:c.174G>A	NP_937816.1:p.Ala58=
NM_198174.2:c.174G>A	NP_937817.3:p.Ala58=
XM_011541869.1:c.36G>A	XP_011540171.1:p.Ala12=
XM_011541870.1:c.-75-3063G>A	XP_011540172.1:n.-75-3063G>A
XM_011541870.2:c.-75-3063G>A	XP_011540172.1:n.-75-3063G>A
NM_001195010.2:c.36G>A	NP_001181939.1:p.Ala12=
NM_198173.3:c.174G>A MANE Select	NP_937816.1:p.Ala58=
NM_198174.3:c.174G>A	NP_937817.3:p.Ala58=
NM_021180.4:c.189G>A	NP_067003.2:p.Ala63=