Canonical Allele Identifier: CA2659857800

Gene: GGCX

Linked Data

• gnomAD v4: 2-85559173-CTTCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85559178_85559182del , CM000664.2:g.85559178_85559182del	GRCh38
NC_000002.11:g.85786301_85786305del , CM000664.1:g.85786301_85786305del	GRCh37
NC_000002.10:g.85639812_85639816del	NCBI36
NG_011811.2:g.7357_7361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482662.2:n.282-103_282-99del
ENST00000496962.2:c.215-103_215-99del	ENSP00000508856.1:n.215-103_215-99del
ENST00000685865.1:n.307-103_307-99del
ENST00000687250.1:n.318-103_318-99del
ENST00000687995.1:n.256-103_256-99del
ENST00000688205.1:c.215-103_215-99del	ENSP00000509673.1:n.215-103_215-99del
ENST00000688788.1:n.307-103_307-99del
ENST00000689276.1:c.215-103_215-99del	ENSP00000510012.1:n.215-103_215-99del
ENST00000689576.1:c.215-103_215-99del	ENSP00000508712.1:n.215-103_215-99del
ENST00000690108.1:c.215-103_215-99del	ENSP00000510617.1:n.215-103_215-99del
ENST00000690468.1:c.44-103_44-99del	ENSP00000509078.1:n.44-103_44-99del
ENST00000690595.1:c.214+1637_214+1641del	ENSP00000508979.1:n.214+1637_214+1641del
ENST00000691348.1:c.44-103_44-99del	ENSP00000509369.1:n.44-103_44-99del
ENST00000691410.1:c.215-103_215-99del	ENSP00000508479.1:n.215-103_215-99del
ENST00000693287.1:c.-67+2208_-67+2212del	ENSP00000510264.1:n.-67+2208_-67+2212del
ENST00000693681.1:c.44-103_44-99del	ENSP00000510789.1:n.44-103_44-99del
ENST00000233838.9:c.215-103_215-99del MANE Select	ENSP00000233838.3:n.215-103_215-99del
ENST00000233838.8:c.215-103_215-99del	ENSP00000233838.3:n.215-103_215-99del
ENST00000421496.5:c.44-103_44-99del	ENSP00000400384.1:n.44-103_44-99del
ENST00000423570.5:c.215-103_215-99del	ENSP00000389426.1:n.215-103_215-99del
ENST00000428479.3:c.44-103_44-99del	ENSP00000390748.3:n.44-103_44-99del
ENST00000430215.7:c.44-103_44-99del	ENSP00000408045.3:n.44-103_44-99del
ENST00000465637.5:n.109-103_109-99del
ENST00000481541.1:n.109-103_109-99del
ENST00000496962.1:n.334-103_334-99del
NM_000821.5:c.215-103_215-99del	NP_000812.2:n.215-103_215-99del
NM_000821.6:c.215-103_215-99del	NP_000812.2:n.215-103_215-99del
NM_001142269.2:c.44-103_44-99del	NP_001135741.1:n.44-103_44-99del
NM_001142269.3:c.44-103_44-99del	NP_001135741.1:n.44-103_44-99del
NM_001311312.1:c.215-103_215-99del	NP_001298241.1:n.215-103_215-99del
XM_005264259.3:c.215-103_215-99del	XP_005264316.1:n.215-103_215-99del
XM_011532764.1:c.-444-103_-444-99del	XP_011531066.1:n.-444-103_-444-99del
XM_011532765.1:c.-444-103_-444-99del	XP_011531067.1:n.-444-103_-444-99del
XR_939677.1:n.280-103_280-99del
XM_005264259.5:c.215-103_215-99del	XP_005264316.1:n.215-103_215-99del
XM_011532764.3:c.-444-103_-444-99del	XP_011531066.1:n.-444-103_-444-99del
XM_011532765.3:c.-444-103_-444-99del	XP_011531067.1:n.-444-103_-444-99del
XM_017003803.2:c.44-103_44-99del	XP_016859292.1:n.44-103_44-99del
XR_001738703.2:n.280-103_280-99del
NM_000821.7:c.215-103_215-99del MANE Select	NP_000812.2:n.215-103_215-99del
NM_001142269.4:c.44-103_44-99del	NP_001135741.1:n.44-103_44-99del
NM_001311312.2:c.215-103_215-99del	NP_001298241.1:n.215-103_215-99del