Canonical Allele Identifier: CA690035
Gene: GRHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.24338084G>A , CM000663.2:g.24338084G>A GRCh38
NC_000001.10:g.24664574G>A , CM000663.1:g.24664574G>A GRCh37
NC_000001.9:g.24537161G>A NCBI36
NG_009308.1:g.23694G>A
NG_009308.2:g.23694G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461318.2:c.933G>A ENSP00000508789.1:p.Lys311=
ENST00000524724.6:c.795G>A ENSP00000431290.2:p.Lys265=
ENST00000528064.6:c.654G>A ENSP00000435130.2:p.Lys218=
ENST00000689444.1:c.795G>A ENSP00000509040.1:p.Lys265=
ENST00000690803.1:c.654G>A ENSP00000510783.1:p.Lys218=
ENST00000692334.1:c.654G>A ENSP00000509790.1:p.Lys218=
ENST00000361548.9:c.933G>A MANE Select ENSP00000354943.5:p.Lys311=
ENST00000236255.4:c.948G>A ENSP00000236255.4:p.Lys316=
ENST00000350501.9:c.933G>A ENSP00000288955.5:p.Lys311=
ENST00000356046.6:c.795G>A ENSP00000348333.2:p.Lys265=
ENST00000361548.8:c.933G>A ENSP00000354943.4:p.Lys311=
ENST00000528064.5:c.*602G>A ENSP00000435130.1:n.*602G>A
ENST00000528181.1:n.385G>A
NM_001195010.1:c.795G>A NP_001181939.1:p.Lys265=
NM_021180.3:c.948G>A NP_067003.2:p.Lys316=
NM_198173.2:c.933G>A NP_937816.1:p.Lys311=
NM_198174.2:c.933G>A NP_937817.3:p.Lys311=
XM_011541869.1:c.795G>A XP_011540171.1:p.Lys265=
XM_011541870.1:c.654G>A XP_011540172.1:p.Lys218=
XM_011541870.2:c.654G>A XP_011540172.1:p.Lys218=
NM_001195010.2:c.795G>A NP_001181939.1:p.Lys265=
NM_198173.3:c.933G>A MANE Select NP_937816.1:p.Lys311=
NM_198174.3:c.933G>A NP_937817.3:p.Lys311=
NM_021180.4:c.948G>A NP_067003.2:p.Lys316=