Canonical Allele Identifier: CA1139848942

Gene: NASP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45618711G= , CM000663.2:g.45618711G=	GRCh38
NC_000001.10:g.46084383G= , CM000663.1:g.46084383G=	GRCh37
NC_000001.9:g.45856970G=	NCBI36
NG_029224.1:g.39724G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002482.4:c.*570G= MANE Select	NP_002473.2:n.*570G=
ENST00000350030.8:c.*570G= MANE Select	ENSP00000255120.5:n.*570G=
NM_001195193.1:c.*570G=	NP_001182122.1:n.*570G=
NM_001195193.2:c.*570G=	NP_001182122.1:n.*570G=
NM_002482.3:c.*570G=	NP_002473.2:n.*570G=
NM_152298.3:c.*570G=	NP_689511.2:n.*570G=
NM_152298.4:c.*570G=	NP_689511.2:n.*570G=
ENST00000350030.7:c.*570G=	ENSP00000255120.5:n.*570G=
ENST00000537798.5:c.*570G=	ENSP00000438871.1:n.*570G=
XM_005270888.2:c.*570G=	XP_005270945.1:n.*570G=
XM_005270888.3:c.*570G=	XP_005270945.1:n.*570G=
XM_005270889.2:c.*570G=	XP_005270946.1:n.*570G=
XM_005270889.3:c.*570G=	XP_005270946.1:n.*570G=
XM_011541509.1:c.*570G=	XP_011539811.1:n.*570G=
XM_011541509.2:c.*570G=	XP_011539811.1:n.*570G=
XM_017001356.2:c.*570G=	XP_016856845.1:n.*570G=