Canonical Allele Identifier: CA2573050969

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41474575_41474910del , CM000685.2:g.41474575_41474910del	GRCh38
NC_000023.10:g.41333828_41334163del , CM000685.1:g.41333828_41334163del	GRCh37
NC_000023.9:g.41218772_41219107del	NCBI36
NG_009112.1:g.32116_32451del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342595.3:c.1107_*11del	ENSP00000340328.3:n.[c.1107_*11del;Ser369ArgfsTer10]
ENST00000378220.3:c.1107_*11del MANE Select	ENSP00000367465.2:n.[c.1107_*11del;Ser369ArgfsTer10]
ENST00000378220.2:c.1122_*11del	ENSP00000367465.1:n.[c.1122_*11del;Ser374ArgfsTer10]
ENST00000342595.2:c.1122_*11del	ENSP00000340328.2:n.[c.1122_*11del;Ser374ArgfsTer10]
ENST00000378220.1:c.1122_*11del	ENSP00000367465.1:n.[c.1122_*11del;Ser374ArgfsTer10]
NM_022567.2:c.1122_*11del	NP_072089.1:n.[c.1122_*11del;Ser374ArgfsTer10]
XM_005272632.2:c.1122_*11del	XP_005272689.1:n.[c.1122_*11del;Ser374ArgfsTer10]
XM_017029709.1:c.1122_*11del	XP_016885198.1:n.[c.1122_*11del;Ser374ArgfsTer10]
NM_001378477.3:c.1107_*11del MANE Select	NP_001365406.2:n.[c.1107_*11del;Ser369ArgfsTer10]
NM_022567.3:c.1107_*11del	NP_072089.2:n.[c.1107_*11del;Ser369ArgfsTer10]