Canonical Allele Identifier: CA371643405

Gene: GRHL2

Linked Data

• MyVariant Identifiers: chr8:g.102555644C>A (hg19) ; chr8:g.101543416C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543416C>A , CM000670.2:g.101543416C>A	GRCh38
NC_000008.10:g.102555644C>A , CM000670.1:g.102555644C>A	GRCh37
NC_000008.9:g.102624820C>A	NCBI36
NG_011971.1:g.55977C>A
NG_011971.2:g.55977C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.196C>A MANE Select	ENSP00000495564.1:p.Leu66Met
ENST00000251808.7:c.196C>A	ENSP00000251808.3:p.Leu66Met
ENST00000395927.1:c.148C>A	ENSP00000379260.1:p.Leu50Met
ENST00000472106.2:n.524C>A
NM_024915.3:c.196C>A	NP_079191.2:p.Leu66Met
XM_011517305.1:c.148C>A	XP_011515607.1:p.Leu50Met
XM_011517306.1:c.148C>A	XP_011515608.1:p.Leu50Met
XM_011517307.1:c.196C>A	XP_011515609.1:p.Leu66Met
NM_001330593.1:c.148C>A	NP_001317522.1:p.Leu50Met
XM_011517306.3:c.148C>A	XP_011515608.1:p.Leu50Met
XM_011517307.3:c.196C>A	XP_011515609.1:p.Leu66Met
NM_001330593.2:c.148C>A	NP_001317522.1:p.Leu50Met
NM_024915.4:c.196C>A MANE Select	NP_079191.2:p.Leu66Met