Canonical Allele Identifier: CA2579220647

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101644242_101644243del , CM000670.2:g.101644242_101644243del	GRCh38
NC_000008.10:g.102656470_102656471del , CM000670.1:g.102656470_102656471del	GRCh37
NC_000008.9:g.102725646_102725647del	NCBI36
NG_011971.1:g.156803_156804del
NG_011971.2:g.156803_156804del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.1612+17_1612+18del MANE Select	ENSP00000495564.1:n.1612+17_1612+18del
ENST00000251808.7:c.1612+17_1612+18del	ENSP00000251808.3:n.1612+17_1612+18del
ENST00000395927.1:c.1564+17_1564+18del	ENSP00000379260.1:n.1564+17_1564+18del
ENST00000474338.1:n.254+17_254+18del
ENST00000517674.5:n.267+17_267+18del
NM_024915.3:c.1612+17_1612+18del	NP_079191.2:n.1612+17_1612+18del
XM_011517305.1:c.1564+17_1564+18del	XP_011515607.1:n.1564+17_1564+18del
XM_011517306.1:c.1564+17_1564+18del	XP_011515608.1:n.1564+17_1564+18del
XM_011517307.1:c.1612+17_1612+18del	XP_011515609.1:n.1612+17_1612+18del
NM_001330593.1:c.1564+17_1564+18del	NP_001317522.1:n.1564+17_1564+18del
XM_011517306.3:c.1564+17_1564+18del	XP_011515608.1:n.1564+17_1564+18del
XM_011517307.3:c.1612+17_1612+18del	XP_011515609.1:n.1612+17_1612+18del
NM_001330593.2:c.1564+17_1564+18del	NP_001317522.1:n.1564+17_1564+18del
NM_024915.4:c.1612+17_1612+18del MANE Select	NP_079191.2:n.1612+17_1612+18del