Canonical Allele Identifier: CA10654310

Gene: NYX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41447611T>C , CM000685.2:g.41447611T>C	GRCh38
NC_000023.10:g.41306864T>C , CM000685.1:g.41306864T>C	GRCh37
NC_000023.9:g.41191808T>C	NCBI36
NG_009112.1:g.5152T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001378477.3:c.-57+95T>C MANE Select	NP_001365406.2:n.-57+95T>C
ENST00000378220.3:c.-57+95T>C MANE Select	ENSP00000367465.2:n.-57+95T>C
NM_022567.2:c.-279T>C	NP_072089.1:n.-279T>C
NM_022567.3:c.-294T>C	NP_072089.2:n.-294T>C
ENST00000342595.2:c.-279T>C	ENSP00000340328.2:n.-279T>C
ENST00000342595.3:c.-294T>C	ENSP00000340328.3:n.-294T>C
ENST00000378220.1:c.-42+95T>C	ENSP00000367465.1:n.-42+95T>C
ENST00000378220.2:c.-42+95T>C	ENSP00000367465.1:n.-42+95T>C
XM_005272632.2:c.-42+95T>C	XP_005272689.1:n.-42+95T>C
XM_017029709.1:c.-42+95T>C	XP_016885198.1:n.-42+95T>C