Canonical Allele Identifier: CA2577020935

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553116_85553119del , CM000664.2:g.85553116_85553119del	GRCh38
NC_000002.11:g.85780239_85780242del , CM000664.1:g.85780239_85780242del	GRCh37
NC_000002.10:g.85633750_85633753del	NCBI36
NG_011811.2:g.13418_13421del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5200-47_5200-44del
ENST00000482662.2:n.3607-47_3607-44del
ENST00000685865.1:n.1559-47_1559-44del
ENST00000687250.1:n.1259-47_1259-44del
ENST00000687995.1:n.1508-47_1508-44del
ENST00000688205.1:c.*749-47_*749-44del	ENSP00000509673.1:n.*749-47_*749-44del
ENST00000688788.1:n.1395-47_1395-44del
ENST00000689276.1:c.1087-47_1087-44del	ENSP00000510012.1:n.1087-47_1087-44del
ENST00000689576.1:c.1156-47_1156-44del	ENSP00000508712.1:n.1156-47_1156-44del
ENST00000690108.1:c.*812-47_*812-44del	ENSP00000510617.1:n.*812-47_*812-44del
ENST00000690468.1:c.877-47_877-44del	ENSP00000509078.1:n.877-47_877-44del
ENST00000690595.1:c.481-47_481-44del	ENSP00000508979.1:n.481-47_481-44del
ENST00000691348.1:c.985-47_985-44del	ENSP00000509369.1:n.985-47_985-44del
ENST00000691410.1:c.*733-47_*733-44del	ENSP00000508479.1:n.*733-47_*733-44del
ENST00000693287.1:c.472-47_472-44del	ENSP00000510264.1:n.472-47_472-44del
ENST00000693681.1:c.469-47_469-44del	ENSP00000510789.1:n.469-47_469-44del
ENST00000233838.9:c.1156-47_1156-44del MANE Select	ENSP00000233838.3:n.1156-47_1156-44del
ENST00000233838.8:c.1156-47_1156-44del	ENSP00000233838.3:n.1156-47_1156-44del
ENST00000430215.7:c.985-47_985-44del	ENSP00000408045.3:n.985-47_985-44del
ENST00000465637.5:n.179-5113_179-5110del
ENST00000473665.1:n.649-47_649-44del
ENST00000482662.1:n.573-47_573-44del
NM_000821.5:c.1156-47_1156-44del	NP_000812.2:n.1156-47_1156-44del
NM_000821.6:c.1156-47_1156-44del	NP_000812.2:n.1156-47_1156-44del
NM_001142269.2:c.985-47_985-44del	NP_001135741.1:n.985-47_985-44del
NM_001142269.3:c.985-47_985-44del	NP_001135741.1:n.985-47_985-44del
XM_005264259.3:c.1156-47_1156-44del	XP_005264316.1:n.1156-47_1156-44del
XM_011532764.1:c.334-47_334-44del	XP_011531066.1:n.334-47_334-44del
XM_011532765.1:c.334-47_334-44del	XP_011531067.1:n.334-47_334-44del
XR_939677.1:n.1221-47_1221-44del
XM_005264259.5:c.1156-47_1156-44del	XP_005264316.1:n.1156-47_1156-44del
XM_011532764.3:c.334-47_334-44del	XP_011531066.1:n.334-47_334-44del
XM_011532765.3:c.334-47_334-44del	XP_011531067.1:n.334-47_334-44del
XM_017003803.2:c.985-47_985-44del	XP_016859292.1:n.985-47_985-44del
XR_001738703.2:n.1221-47_1221-44del
NM_000821.7:c.1156-47_1156-44del MANE Select	NP_000812.2:n.1156-47_1156-44del
NM_001142269.4:c.985-47_985-44del	NP_001135741.1:n.985-47_985-44del