Canonical Allele Identifier: CA454019373

Gene: GSDME

Linked Data

• MyVariant Identifiers: chr7:g.24745804T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24706185T>A , CM000669.2:g.24706185T>A	GRCh38
NC_000007.13:g.24745804T>A , CM000669.1:g.24745804T>A	GRCh37
NC_000007.12:g.24712329T>A	NCBI36
NG_011593.1:g.56836A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342947.9:c.1182A>T	ENSP00000339587.3:p.Ala394=
ENST00000409970.6:c.690A>T	ENSP00000387119.1:p.Ala230=
ENST00000419307.6:c.690A>T	ENSP00000401332.1:p.Ala230=
ENST00000645220.1:c.1182A>T MANE Select	ENSP00000494186.1:p.Ala394=
ENST00000342947.7:c.1182A>T	ENSP00000339587.3:p.Ala394=
ENST00000409775.7:c.1182A>T	ENSP00000386670.3:p.Ala394=
ENST00000409970.5:c.690A>T	ENSP00000387119.1:p.Ala230=
ENST00000419307.5:c.690A>T	ENSP00000401332.1:p.Ala230=
ENST00000430096.1:c.42A>T	ENSP00000395540.1:p.Ala14=
NM_001127453.1:c.1182A>T	NP_001120925.1:p.Ala394=
NM_001127454.1:c.690A>T	NP_001120926.1:p.Ala230=
NM_004403.2:c.1182A>T	NP_004394.1:p.Ala394=
XM_017011802.1:c.690A>T	XP_016867291.1:p.Ala230=
XM_024446670.1:c.1182A>T	XP_024302438.1:p.Ala394=
NM_004403.3:c.1182A>T	NP_004394.1:p.Ala394=
NM_001127453.2:c.1182A>T MANE Select	NP_001120925.1:p.Ala394=
NM_001127454.2:c.690A>T	NP_001120926.1:p.Ala230=