Canonical Allele Identifier: CA412024654
Gene: ANOS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731993C>G , CM000685.2:g.8731993C>G GRCh38
NC_000023.10:g.8700034C>G , CM000685.1:g.8700034C>G GRCh37
NC_000023.9:g.8660034C>G NCBI36
NG_007088.1:g.5194G>C
NG_007088.2:g.5194G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.44G>C MANE Select ENSP00000262648.3:p.Trp15Ser
ENST00000262648.7:c.44G>C ENSP00000262648.3:p.Trp15Ser
ENST00000619786.1:c.44G>C ENSP00000478734.1:p.Trp15Ser
NM_000216.2:c.44G>C NP_000207.2:p.Trp15Ser
XM_005274501.3:c.44G>C XP_005274558.1:p.Trp15Ser
NM_000216.3:c.44G>C NP_000207.2:p.Trp15Ser
XM_005274501.4:c.44G>C XP_005274558.1:p.Trp15Ser
NM_000216.4:c.44G>C MANE Select NP_000207.2:p.Trp15Ser