Canonical Allele Identifier: CA371591698

Gene: GRHL2

Linked Data

• MyVariant Identifiers: chr8:g.102656363A>T (hg19) ; chr8:g.101644135A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101644135A>T , CM000670.2:g.101644135A>T	GRCh38
NC_000008.10:g.102656363A>T , CM000670.1:g.102656363A>T	GRCh37
NC_000008.9:g.102725539A>T	NCBI36
NG_011971.1:g.156696A>T
NG_011971.2:g.156696A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.1522A>T MANE Select	ENSP00000495564.1:p.Ser508Cys
ENST00000251808.7:c.1522A>T	ENSP00000251808.3:p.Ser508Cys
ENST00000395927.1:c.1474A>T	ENSP00000379260.1:p.Ser492Cys
ENST00000474338.1:n.164A>T
ENST00000517674.5:n.177A>T
NM_024915.3:c.1522A>T	NP_079191.2:p.Ser508Cys
XM_011517305.1:c.1474A>T	XP_011515607.1:p.Ser492Cys
XM_011517306.1:c.1474A>T	XP_011515608.1:p.Ser492Cys
XM_011517307.1:c.1522A>T	XP_011515609.1:p.Ser508Cys
NM_001330593.1:c.1474A>T	NP_001317522.1:p.Ser492Cys
XM_011517306.3:c.1474A>T	XP_011515608.1:p.Ser492Cys
XM_011517307.3:c.1522A>T	XP_011515609.1:p.Ser508Cys
NM_001330593.2:c.1474A>T	NP_001317522.1:p.Ser492Cys
NM_024915.4:c.1522A>T MANE Select	NP_079191.2:p.Ser508Cys