Canonical Allele Identifier: CA367047951

Gene: GSDME

Linked Data

• gnomAD v4: 7-24717294-G-T
• MyVariant Identifiers: chr7:g.24756913G>T (hg19) ; chr7:g.24717294G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24717294G>T , CM000669.2:g.24717294G>T	GRCh38
NC_000007.13:g.24756913G>T , CM000669.1:g.24756913G>T	GRCh37
NC_000007.12:g.24723438G>T	NCBI36
NG_011593.1:g.45727C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342947.9:c.657C>A	ENSP00000339587.3:p.Tyr219Ter
ENST00000409970.6:c.165C>A	ENSP00000387119.1:p.Tyr55Ter
ENST00000411476.3:n.426C>A
ENST00000414428.2:c.657C>A	ENSP00000413963.2:p.Tyr219Ter
ENST00000419307.6:c.165C>A	ENSP00000401332.1:p.Tyr55Ter
ENST00000446822.6:c.131C>A
ENST00000559637.6:n.352C>A
ENST00000645220.1:c.657C>A MANE Select	ENSP00000494186.1:p.Tyr219Ter
ENST00000342947.7:c.657C>A	ENSP00000339587.3:p.Tyr219Ter
ENST00000409775.7:c.657C>A	ENSP00000386670.3:p.Tyr219Ter
ENST00000409970.5:c.165C>A	ENSP00000387119.1:p.Tyr55Ter
ENST00000411476.2:c.426C>A	ENSP00000414090.2:p.Tyr142Ter
ENST00000415480.5:c.23C>A
ENST00000419307.5:c.165C>A	ENSP00000401332.1:p.Tyr55Ter
ENST00000446822.5:c.131C>A
ENST00000493723.5:n.676C>A
ENST00000559637.5:n.352C>A
NM_001127453.1:c.657C>A	NP_001120925.1:p.Tyr219Ter
NM_001127454.1:c.165C>A	NP_001120926.1:p.Tyr55Ter
NM_004403.2:c.657C>A	NP_004394.1:p.Tyr219Ter
XM_017011802.1:c.165C>A	XP_016867291.1:p.Tyr55Ter
XM_024446670.1:c.657C>A	XP_024302438.1:p.Tyr219Ter
NM_004403.3:c.657C>A	NP_004394.1:p.Tyr219Ter
NM_001127453.2:c.657C>A MANE Select	NP_001120925.1:p.Tyr219Ter
NM_001127454.2:c.165C>A	NP_001120926.1:p.Tyr55Ter