Canonical Allele Identifier: CA10901392
Gene: NASP HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1053941

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_001195193.1:c.*570G>T VV NP_001182122.1:p.=
NM_002482.3:c.*570G>T VV NP_002473.2:p.=
NM_152298.3:c.*570G>T VV NP_689511.2:p.=
XM_005270888.2:c.*570G>T XP_005270945.1:p.=
XM_005270889.2:c.*570G>T XP_005270946.1:p.=
XM_011541509.1:c.*570G>T XP_011539811.1:p.=
XM_005270888.3:c.*570G>T
XM_005270889.3:c.*570G>T
XM_011541509.2:c.*570G>T
XM_017001356.2:c.*570G>T XP_016856845.1:p.=
ENST00000350030.7:c.*570G>T ENSP00000255120.5:p.=
ENST00000537798.5:c.*570G>T ENSP00000438871.1:p.=